Canonical Allele Identifier: CA375686101

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131549T>A (hg19) ; chr9:g.133256162T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256162T>A , CM000671.2:g.133256162T>A	GRCh38
NC_000009.11:g.136131549T>A , CM000671.1:g.136131549T>A	GRCh37
NC_000009.10:g.135121370T>A	NCBI36
NG_006669.1:g.21506A>T
NG_006669.2:g.24054A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.598A>T
ENST00000647353.1:n.54-5010A>T
ENST00000651471.1:n.524A>T
ENST00000679909.1:c.28+19000A>T	ENSP00000506089.1:n.28+19000A>T
ENST00000453660.3:n.580A>T
ENST00000538324.2:c.566A>T	ENSP00000483018.1:p.Glu189Val
ENST00000611156.4:c.566A>T	ENSP00000483265.1:p.Glu189Val
NM_020469.2:c.569A>T	NP_065202.2:p.Glu190Val
NM_020469.3:c.569A>T	NP_065202.2:p.Glu190Val