Canonical Allele Identifier: CA375686794

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132923C>A (hg19) ; chr9:g.133257536C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257536C>A , CM000671.2:g.133257536C>A	GRCh38
NC_000009.11:g.136132923C>A , CM000671.1:g.136132923C>A	GRCh37
NC_000009.10:g.135122744C>A	NCBI36
NG_006669.1:g.20131G>T
NG_006669.2:g.22679G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.276G>T
ENST00000647353.1:n.54-6384G>T
ENST00000651471.1:n.329+506G>T
ENST00000679909.1:c.28+17626G>T	ENSP00000506089.1:n.28+17626G>T
ENST00000453660.3:n.258G>T
ENST00000538324.2:c.246G>T	ENSP00000483018.1:p.Lys82Asn
ENST00000611156.4:c.246G>T	ENSP00000483265.1:p.Lys82Asn
NM_020469.2:c.246G>T	NP_065202.2:p.Lys82Asn
NM_020469.3:c.246G>T	NP_065202.2:p.Lys82Asn