Canonical Allele Identifier: CA1882582704

Gene: ABO

Linked Data

• dbSNP Id: rs1834629198

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257733T>G , CM000671.2:g.133257733T>G	GRCh38
NC_000009.11:g.136133120T>G , CM000671.1:g.136133120T>G	GRCh37
NC_000009.10:g.135122941T>G	NCBI36
NG_006669.1:g.19934A>C
NG_006669.2:g.22482A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.270-191A>C
ENST00000647353.1:n.54-6581A>C
ENST00000651471.1:n.329+309A>C
ENST00000679909.1:c.28+17429A>C	ENSP00000506089.1:n.28+17429A>C
ENST00000453660.3:n.252-191A>C
ENST00000538324.2:c.240-191A>C	ENSP00000483018.1:n.240-191A>C
ENST00000611156.4:c.240-191A>C	ENSP00000483265.1:n.240-191A>C
NM_020469.2:c.240-191A>C	NP_065202.2:n.240-191A>C
NM_020469.3:c.240-191A>C	NP_065202.2:n.240-191A>C