Canonical Allele Identifier: CA2786163082

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256182_133256183insA , CM000671.2:g.133256182_133256183insA	GRCh38
NC_000009.11:g.136131569_136131570insA , CM000671.1:g.136131569_136131570insA	GRCh37
NC_000009.10:g.135121390_135121391insA	NCBI36
NG_006669.1:g.21485_21486insT
NG_006669.2:g.24033_24034insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.577_578insT
ENST00000647353.1:n.54-5031_54-5030insT
ENST00000651471.1:n.503_504insT
ENST00000679909.1:c.28+18979_28+18980insT	ENSP00000506089.1:n.28+18979_28+18980insT
ENST00000453660.3:n.559_560insT
ENST00000538324.2:c.545_546insT	ENSP00000483018.1:p.Val183ArgfsTer11
ENST00000611156.4:c.545_546insT	ENSP00000483265.1:p.Val183ArgfsTer11
NM_020469.2:c.548_549insT	NP_065202.2:p.Val184ArgfsTer11
NM_020469.3:c.548_549insT	NP_065202.2:p.Val184ArgfsTer11