Canonical Allele Identifier: CA1882580391

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256115A= , CM000671.2:g.133256115A=	GRCh38
NC_000009.11:g.136131502A= , CM000671.1:g.136131502A=	GRCh37
NC_000009.10:g.135121323A=	NCBI36
NG_006669.1:g.21553T=
NG_006669.2:g.24101T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.645T=
ENST00000647353.1:n.54-4963T=
ENST00000651471.1:n.571T=
ENST00000679909.1:c.28+19047T=	ENSP00000506089.1:n.28+19047T=
ENST00000453660.3:n.627T=
ENST00000538324.2:c.613T=	ENSP00000483018.1:p.Tyr205=
ENST00000611156.4:c.613T=	ENSP00000483265.1:p.Tyr205=
NM_020469.2:c.616T=	NP_065202.2:p.Tyr206=
NM_020469.3:c.616T=	NP_065202.2:p.Tyr206=