Canonical Allele Identifier: CA5305841
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782329950

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256268G>A , CM000671.2:g.133256268G>A GRCh38
NC_000009.11:g.136131655G>A , CM000671.1:g.136131655G>A GRCh37
NC_000009.10:g.135121476G>A NCBI36
NG_006669.1:g.21400C>T
NG_006669.2:g.23948C>T

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.463C>T NP_065202.2:p.Gln155Ter
NM_020469.3:c.463C>T NP_065202.2:p.Gln155Ter
ENST00000453660.3:n.474C>T
ENST00000538324.2:c.460C>T ENSP00000483018.1:p.Gln154Ter
ENST00000611156.4:c.460C>T ENSP00000483265.1:p.Gln154Ter