Canonical Allele Identifier: CA1882590519

Gene: ABO

Linked Data

• dbSNP Id: rs1834957071

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274056A>G , CM000671.2:g.133274056A>G	GRCh38
NC_000009.11:g.136149472A>G , CM000671.1:g.136149472A>G	GRCh37
NC_000009.10:g.135139293A>G	NCBI36
NG_006669.1:g.3579T>C
NG_006669.2:g.6159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.58+1106T>C
ENST00000647353.1:n.53+1106T>C
ENST00000651471.1:n.63+1906T>C
ENST00000679909.1:c.28+1106T>C	ENSP00000506089.1:n.28+1106T>C
ENST00000453660.3:n.40+1106T>C
ENST00000538324.2:c.28+1106T>C	ENSP00000483018.1:n.28+1106T>C
ENST00000611156.4:c.28+1106T>C	ENSP00000483265.1:n.28+1106T>C
NM_020469.2:c.28+1106T>C	NP_065202.2:n.28+1106T>C
NM_020469.3:c.28+1106T>C	NP_065202.2:n.28+1106T>C