Canonical Allele Identifier: CA467780088

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130720T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255333T>A , CM000671.2:g.133255333T>A	GRCh38
NC_000009.11:g.136130720T>A , CM000671.1:g.136130720T>A	GRCh37
NC_000009.10:g.135120541T>A	NCBI36
NG_006669.1:g.22335A>T
NG_006669.2:g.24883A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1427A>T
ENST00000647353.1:n.54-4181A>T
ENST00000679909.1:c.28+19829A>T	ENSP00000506089.1:n.28+19829A>T
ENST00000453660.3:n.1409A>T
ENST00000611156.4:c.*333A>T	ENSP00000483265.1:n.*333A>T
NM_020469.2:c.*333A>T	NP_065202.2:n.*333A>T
NM_020469.3:c.*333A>T	NP_065202.2:n.*333A>T