Canonical Allele Identifier: CA375686247

Gene: ABO

Linked Data

• dbSNP Id: rs782734774
• MyVariant Identifiers: chr9:g.136131622T>C (hg19) ; chr9:g.133256235T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256235T>C , CM000671.2:g.133256235T>C	GRCh38
NC_000009.11:g.136131622T>C , CM000671.1:g.136131622T>C	GRCh37
NC_000009.10:g.135121443T>C	NCBI36
NG_006669.1:g.21433A>G
NG_006669.2:g.23981A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.525A>G
ENST00000647353.1:n.54-5083A>G
ENST00000651471.1:n.451A>G
ENST00000679909.1:c.28+18927A>G	ENSP00000506089.1:n.28+18927A>G
ENST00000453660.3:n.507A>G
ENST00000538324.2:c.493A>G	ENSP00000483018.1:p.Thr165Ala
ENST00000611156.4:c.493A>G	ENSP00000483265.1:p.Thr165Ala
NM_020469.2:c.496A>G	NP_065202.2:p.Thr166Ala
NM_020469.3:c.496A>G	NP_065202.2:p.Thr166Ala