Canonical Allele Identifier: CA1882581958

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257016C= , CM000671.2:g.133257016C=	GRCh38
NC_000009.11:g.136132403C= , CM000671.1:g.136132403C=	GRCh37
NC_000009.10:g.135122224C=	NCBI36
NG_006669.1:g.20652G=
NG_006669.2:g.23200G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.403+393G=
ENST00000647353.1:n.54-5864G=
ENST00000651471.1:n.330-660G=
ENST00000679909.1:c.28+18146G=	ENSP00000506089.1:n.28+18146G=
ENST00000453660.3:n.385+393G=
ENST00000538324.2:c.371+393G=	ENSP00000483018.1:n.371+393G=
ENST00000611156.4:c.371+393G=	ENSP00000483265.1:n.371+393G=
NM_020469.2:c.374+393G=	NP_065202.2:n.374+393G=
NM_020469.3:c.374+393G=	NP_065202.2:n.374+393G=