Table 2.
Information content of the BGMUT resourcea
| Gene alleles | amino acid sequence variation |
| contributor | |
| examined gene regionsb (67%) | |
| name and aliases | |
| nucleotide sequence variation | |
| phenotype (89%) | |
| prevalence in population (90%) | |
| published referencec (93%) | |
| sequence identifier (ID) in sequence repositories (43%) | |
| unique allele ID in BGMUT | |
| Blood group systems | contributing experts |
| disease association | |
| genes and proteins | |
| IDs for other databases like OMIM and dbSNP | |
| introduction | |
| nature of gene variation | |
| reference sequence IDs | |
| serological aspects | |
| Other | carbohydrate blood group antigens like CAD and Sid |
| links to resources | |
| orthologous ABO, MNS and RH systems | |
| non-erythroid RHAG gene homologs | |
| tutorials | |
a
As on 24 March 2014.
b
Percentage of non-reference alleles for which such information is available.
c
94% of the publications are indexed in the PubMed database