Canonical Allele Identifier: CA375686306

Gene: ABO

Linked Data

• dbSNP Id: rs1834581164
• MyVariant Identifiers: chr9:g.136131654T>G (hg19) ; chr9:g.133256267T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256267T>G , CM000671.2:g.133256267T>G	GRCh38
NC_000009.11:g.136131654T>G , CM000671.1:g.136131654T>G	GRCh37
NC_000009.10:g.135121475T>G	NCBI36
NG_006669.1:g.21401A>C
NG_006669.2:g.23949A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.493A>C
ENST00000647353.1:n.54-5115A>C
ENST00000651471.1:n.419A>C
ENST00000679909.1:c.28+18895A>C	ENSP00000506089.1:n.28+18895A>C
ENST00000453660.3:n.475A>C
ENST00000538324.2:c.461A>C	ENSP00000483018.1:p.Gln154Pro
ENST00000611156.4:c.461A>C	ENSP00000483265.1:p.Gln154Pro
NM_020469.2:c.464A>C	NP_065202.2:p.Gln155Pro
NM_020469.3:c.464A>C	NP_065202.2:p.Gln155Pro