Canonical Allele Identifier: CA040692

Gene: ABO

Linked Data

• PubMed: PMID:6775529 ; PMID:8456556 ; PMID:14170898

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.[133255928C>G;133256264G>A] , CM000671.2:g.[133255928C>G;133256264G>A]	GRCh38
NC_000009.11:g.[136131315C>G;136131651G>A] , CM000671.1:g.[136131315C>G;136131651G>A]	GRCh37
NC_000009.10:g.[135121136C>G;135121472G>A]	NCBI36
NG_006669.1:g.[21404C>T;21740G>C]
NG_006669.2:g.[23952C>T;24288G>C]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.[496C>T;832G>C]
ENST00000647353.1:n.[54-5112C>T;54-4776G>C]
ENST00000679909.1:c.[28+18898C>T;28+19234G>C]	ENSP00000506089.1:n.[28+18898C>T;28+19234G>C]
ENST00000453660.3:n.[478C>T;814G>C]
ENST00000538324.2:c.[464C>T;800G>C]	ENSP00000483018.1:p.[Pro155Leu;Gly267Ala]
ENST00000611156.4:c.[464C>T;800G>C]	ENSP00000483265.1:p.[Pro155Leu;Gly267Ala]
NM_020469.2:c.[467C>T;803G>C]	NP_065202.2:p.[Pro156Leu;Gly268Ala]
NM_020469.3:c.[467C>T;803G>C]	NP_065202.2:p.[Pro156Leu;Gly268Ala]