Canonical Allele Identifier: CA375685553

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131427T>A (hg19) ; chr9:g.133256040T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256040T>A , CM000671.2:g.133256040T>A	GRCh38
NC_000009.11:g.136131427T>A , CM000671.1:g.136131427T>A	GRCh37
NC_000009.10:g.135121248T>A	NCBI36
NG_006669.1:g.21628A>T
NG_006669.2:g.24176A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.720A>T
ENST00000647353.1:n.54-4888A>T
ENST00000679909.1:c.28+19122A>T	ENSP00000506089.1:n.28+19122A>T
ENST00000453660.3:n.702A>T
ENST00000538324.2:c.688A>T	ENSP00000483018.1:p.Thr230Ser
ENST00000611156.4:c.688A>T	ENSP00000483265.1:p.Thr230Ser
NM_020469.2:c.691A>T	NP_065202.2:p.Thr231Ser
NM_020469.3:c.691A>T	NP_065202.2:p.Thr231Ser