Canonical Allele Identifier: CA375686455

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131720A>T (hg19) ; chr9:g.133256333A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256333A>T , CM000671.2:g.133256333A>T	GRCh38
NC_000009.11:g.136131720A>T , CM000671.1:g.136131720A>T	GRCh37
NC_000009.10:g.135121541A>T	NCBI36
NG_006669.1:g.21335T>A
NG_006669.2:g.23883T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.427T>A
ENST00000647353.1:n.54-5181T>A
ENST00000651471.1:n.353T>A
ENST00000679909.1:c.28+18829T>A	ENSP00000506089.1:n.28+18829T>A
ENST00000453660.3:n.409T>A
ENST00000538324.2:c.395T>A	ENSP00000483018.1:p.Phe132Tyr
ENST00000611156.4:c.395T>A	ENSP00000483265.1:p.Phe132Tyr
NM_020469.2:c.398T>A	NP_065202.2:p.Phe133Tyr
NM_020469.3:c.398T>A	NP_065202.2:p.Phe133Tyr