Canonical Allele Identifier: CA2786163900

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274144_133274145insA , CM000671.2:g.133274144_133274145insA	GRCh38
NC_000009.11:g.136149560_136149561insA , CM000671.1:g.136149560_136149561insA	GRCh37
NC_000009.10:g.135139381_135139382insA	NCBI36
NG_006669.1:g.3490_3491insT
NG_006669.2:g.6070_6071insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.58+1017_58+1018insT
ENST00000647353.1:n.53+1017_53+1018insT
ENST00000651471.1:n.63+1817_63+1818insT
ENST00000679909.1:c.28+1017_28+1018insT	ENSP00000506089.1:n.28+1017_28+1018insT
ENST00000453660.3:n.40+1017_40+1018insT
ENST00000538324.2:c.28+1017_28+1018insT	ENSP00000483018.1:n.28+1017_28+1018insT
ENST00000611156.4:c.28+1017_28+1018insT	ENSP00000483265.1:n.28+1017_28+1018insT
NM_020469.2:c.28+1017_28+1018insT	NP_065202.2:n.28+1017_28+1018insT
NM_020469.3:c.28+1017_28+1018insT	NP_065202.2:n.28+1017_28+1018insT