Canonical Allele Identifier: CA375686755

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132904G>T (hg19) ; chr9:g.133257517G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257517G>T , CM000671.2:g.133257517G>T	GRCh38
NC_000009.11:g.136132904G>T , CM000671.1:g.136132904G>T	GRCh37
NC_000009.10:g.135122725G>T	NCBI36
NG_006669.1:g.20151C>A
NG_006669.2:g.22699C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.295C>A
ENST00000647353.1:n.54-6365C>A
ENST00000651471.1:n.329+525C>A
ENST00000679909.1:c.28+17645C>A	ENSP00000506089.1:n.28+17645C>A
ENST00000453660.3:n.277C>A
ENST00000538324.2:c.263C>A	ENSP00000483018.1:p.Pro88His
ENST00000611156.4:c.263C>A	ENSP00000483265.1:p.Pro88His
NM_020469.2:c.266C>A	NP_065202.2:p.Pro89His
NM_020469.3:c.266C>A	NP_065202.2:p.Pro89His