Canonical Allele Identifier: CA467782873

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131587G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256200G>T , CM000671.2:g.133256200G>T	GRCh38
NC_000009.11:g.136131587G>T , CM000671.1:g.136131587G>T	GRCh37
NC_000009.10:g.135121408G>T	NCBI36
NG_006669.1:g.21468C>A
NG_006669.2:g.24016C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.560C>A
ENST00000647353.1:n.54-5048C>A
ENST00000651471.1:n.486C>A
ENST00000679909.1:c.28+18962C>A	ENSP00000506089.1:n.28+18962C>A
ENST00000453660.3:n.542C>A
ENST00000538324.2:c.528C>A	ENSP00000483018.1:p.Ala176=
ENST00000611156.4:c.528C>A	ENSP00000483265.1:p.Ala176=
NM_020469.2:c.531C>A	NP_065202.2:p.Ala177=
NM_020469.3:c.531C>A	NP_065202.2:p.Ala177=