Canonical Allele Identifier: CA375686762

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132908T>A (hg19) ; chr9:g.133257521T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257521T>A , CM000671.2:g.133257521T>A	GRCh38
NC_000009.11:g.136132908T>A , CM000671.1:g.136132908T>A	GRCh37
NC_000009.10:g.135122729T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.291A>T
ENST00000647353.1:n.54-6369A>T
ENST00000651471.1:n.329+521A>T
ENST00000679909.1:c.28+17641A>T	ENSP00000506089.1:n.28+17641A>T
ENST00000453660.3:n.273A>T
ENST00000538324.2:c.259A>T	ENSP00000483018.1:p.Thr87Ser
ENST00000611156.4:c.259A>T	ENSP00000483265.1:p.Thr87Ser