Canonical Allele Identifier: CA375682272

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131042C>A (hg19) ; chr9:g.133255655C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255655C>A , CM000671.2:g.133255655C>A	GRCh38
NC_000009.11:g.136131042C>A , CM000671.1:g.136131042C>A	GRCh37
NC_000009.10:g.135120863C>A	NCBI36
NG_006669.1:g.22013G>T
NG_006669.2:g.24561G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1105G>T
ENST00000647353.1:n.54-4503G>T
ENST00000679909.1:c.28+19507G>T	ENSP00000506089.1:n.28+19507G>T
ENST00000453660.3:n.1087G>T
ENST00000538324.2:c.1069G>T	ENSP00000483018.1:p.Gly357Trp
ENST00000611156.4:c.*11G>T	ENSP00000483265.1:n.*11G>T
NM_020469.2:c.*11G>T	NP_065202.2:n.*11G>T
NM_020469.3:c.*11G>T	NP_065202.2:n.*11G>T