Canonical Allele Identifier: CA200766349

Gene: ABO

Linked Data

• dbSNP Id: rs1834633476

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257994del , CM000671.2:g.133257994del	GRCh38
NC_000009.11:g.136133384del , CM000671.1:g.136133384del	GRCh37
NC_000009.10:g.135123205del	NCBI36
NG_006669.1:g.19670del
NG_006669.2:g.22221del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+103del
ENST00000647353.1:n.54-6842del
ENST00000651471.1:n.329+48del
ENST00000679909.1:c.28+17168del	ENSP00000506089.1:n.28+17168del
ENST00000453660.3:n.251+103del
ENST00000538324.2:c.239+103del	ENSP00000483018.1:n.239+103del
ENST00000611156.4:c.239+103del	ENSP00000483265.1:n.239+103del
NM_020469.2:c.239+103del	NP_065202.2:n.239+103del
NM_020469.3:c.239+103del	NP_065202.2:n.239+103del