Canonical Allele Identifier: CA1882578608

Gene: ABO

Linked Data

• dbSNP Id: rs1834547394

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255398_133255407del , CM000671.2:g.133255398_133255407del	GRCh38
NC_000009.11:g.136130785_136130794del , CM000671.1:g.136130785_136130794del	GRCh37
NC_000009.10:g.135120606_135120615del	NCBI36
NG_006669.1:g.22268_22277del
NG_006669.2:g.24816_24825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1360_1369del
ENST00000647353.1:n.54-4248_54-4239del
ENST00000679909.1:c.28+19762_28+19771del	ENSP00000506089.1:n.28+19762_28+19771del
ENST00000453660.3:n.1342_1351del
ENST00000611156.4:c.*266_*275del	ENSP00000483265.1:n.*266_*275del
NM_020469.2:c.*266_*275del	NP_065202.2:n.*266_*275del
NM_020469.3:c.*266_*275del	NP_065202.2:n.*266_*275del