Canonical Allele Identifier: CA467782025

Gene: ABO

Linked Data

• dbSNP Id: rs1834555295
• MyVariant Identifiers: chr9:g.136130998A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255611A>G , CM000671.2:g.133255611A>G	GRCh38
NC_000009.11:g.136130998A>G , CM000671.1:g.136130998A>G	GRCh37
NC_000009.10:g.135120819A>G	NCBI36
NG_006669.1:g.22057T>C
NG_006669.2:g.24605T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1149T>C
ENST00000647353.1:n.54-4459T>C
ENST00000679909.1:c.28+19551T>C	ENSP00000506089.1:n.28+19551T>C
ENST00000453660.3:n.1131T>C
ENST00000538324.2:c.1113T>C	ENSP00000483018.1:p.Pro371=
ENST00000611156.4:c.*55T>C	ENSP00000483265.1:n.*55T>C
NM_020469.2:c.*55T>C	NP_065202.2:n.*55T>C
NM_020469.3:c.*55T>C	NP_065202.2:n.*55T>C