Canonical Allele Identifier: CA200766400

Gene: ABO

Linked Data

• dbSNP Id: rs887020677
• MyVariant Identifiers: chr9:g.136133515A>G (hg19) ; chr9:g.133258125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258125A>G , CM000671.2:g.133258125A>G	GRCh38
NC_000009.11:g.136133515A>G , CM000671.1:g.136133515A>G	GRCh37
NC_000009.10:g.135123336A>G	NCBI36
NG_006669.1:g.19539T>C
NG_006669.2:g.22090T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.241T>C
ENST00000647353.1:n.54-6973T>C
ENST00000651471.1:n.246T>C
ENST00000679909.1:c.28+17037T>C	ENSP00000506089.1:n.28+17037T>C
ENST00000453660.3:n.223T>C
ENST00000538324.2:c.211T>C	ENSP00000483018.1:p.Tyr71His
ENST00000611156.4:c.211T>C	ENSP00000483265.1:p.Tyr71His
NM_020469.2:c.211T>C	NP_065202.2:p.Tyr71His
NM_020469.3:c.211T>C	NP_065202.2:p.Tyr71His