Canonical Allele Identifier: CA1882580965

Gene: ABO

Linked Data

• dbSNP Id: rs1834582677

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256335_133256346del , CM000671.2:g.133256335_133256346del	GRCh38
NC_000009.11:g.136131722_136131733del , CM000671.1:g.136131722_136131733del	GRCh37
NC_000009.10:g.135121543_135121554del	NCBI36
NG_006669.1:g.21328_21339del
NG_006669.2:g.23876_23887del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.420_431del
ENST00000647353.1:n.54-5188_54-5177del
ENST00000651471.1:n.346_357del
ENST00000679909.1:c.28+18822_28+18833del	ENSP00000506089.1:n.28+18822_28+18833del
ENST00000453660.3:n.402_413del
ENST00000538324.2:c.388_399del	ENSP00000483018.1:p.Lys130_Leu133del
ENST00000611156.4:c.388_399del	ENSP00000483265.1:p.Lys130_Leu133del
NM_020469.2:c.391_402del	NP_065202.2:p.Lys131_Leu134del
NM_020469.3:c.391_402del	NP_065202.2:p.Lys131_Leu134del