Canonical Allele Identifier: CA375684128
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255806A>C , CM000671.2:g.133255806A>C GRCh38
NC_000009.11:g.136131193A>C , CM000671.1:g.136131193A>C GRCh37
NC_000009.10:g.135121014A>C NCBI36
NG_006669.1:g.21862T>G
NG_006669.2:g.24410T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.954T>G
ENST00000647353.1:n.54-4654T>G
ENST00000679909.1:c.28+19356T>G ENSP00000506089.1:n.28+19356T>G
ENST00000453660.3:n.936T>G
ENST00000538324.2:c.922T>G ENSP00000483018.1:p.Tyr308Asp
ENST00000611156.4:c.922T>G ENSP00000483265.1:p.Tyr308Asp
NM_020469.2:c.925T>G NP_065202.2:p.Tyr309Asp
NM_020469.3:c.925T>G NP_065202.2:p.Tyr309Asp