Canonical Allele Identifier: CA375686135

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131565A>T (hg19) ; chr9:g.133256178A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256178A>T , CM000671.2:g.133256178A>T	GRCh38
NC_000009.11:g.136131565A>T , CM000671.1:g.136131565A>T	GRCh37
NC_000009.10:g.135121386A>T	NCBI36
NG_006669.1:g.21490T>A
NG_006669.2:g.24038T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.582T>A
ENST00000647353.1:n.54-5026T>A
ENST00000651471.1:n.508T>A
ENST00000679909.1:c.28+18984T>A	ENSP00000506089.1:n.28+18984T>A
ENST00000453660.3:n.564T>A
ENST00000538324.2:c.550T>A	ENSP00000483018.1:p.Ser184Thr
ENST00000611156.4:c.550T>A	ENSP00000483265.1:p.Ser184Thr
NM_020469.2:c.553T>A	NP_065202.2:p.Ser185Thr
NM_020469.3:c.553T>A	NP_065202.2:p.Ser185Thr