Canonical Allele Identifier: CA375686305
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256267T>C , CM000671.2:g.133256267T>C GRCh38
NC_000009.11:g.136131654T>C , CM000671.1:g.136131654T>C GRCh37
NC_000009.10:g.135121475T>C NCBI36
NG_006669.1:g.21401A>G
NG_006669.2:g.23949A>G

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.464A>G NP_065202.2:p.Gln155Arg
NM_020469.3:c.464A>G NP_065202.2:p.Gln155Arg
ENST00000453660.3:n.475A>G
ENST00000538324.2:c.461A>G ENSP00000483018.1:p.Gln154Arg
ENST00000611156.4:c.461A>G ENSP00000483265.1:p.Gln154Arg