Canonical Allele Identifier: CA375686311

Gene: ABO

Linked Data

• dbSNP Id: rs1834581399
• MyVariant Identifiers: chr9:g.136131657T>A (hg19) ; chr9:g.133256270T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256270T>A , CM000671.2:g.133256270T>A	GRCh38
NC_000009.11:g.136131657T>A , CM000671.1:g.136131657T>A	GRCh37
NC_000009.10:g.135121478T>A	NCBI36
NG_006669.1:g.21398A>T
NG_006669.2:g.23946A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.490A>T
ENST00000647353.1:n.54-5118A>T
ENST00000651471.1:n.416A>T
ENST00000679909.1:c.28+18892A>T	ENSP00000506089.1:n.28+18892A>T
ENST00000453660.3:n.472A>T
ENST00000538324.2:c.458A>T	ENSP00000483018.1:p.Asp153Val
ENST00000611156.4:c.458A>T	ENSP00000483265.1:p.Asp153Val
NM_020469.2:c.461A>T	NP_065202.2:p.Asp154Val
NM_020469.3:c.461A>T	NP_065202.2:p.Asp154Val