Canonical Allele Identifier: CA1882585023

Gene: ABO

Linked Data

• dbSNP Id: rs1834712353

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261613C>A , CM000671.2:g.133261613C>A	GRCh38
NC_000009.11:g.136137016C>A , CM000671.1:g.136137016C>A	GRCh37
NC_000009.10:g.135126837C>A	NCBI36
NG_006669.1:g.16037G>T
NG_006669.2:g.18602G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.129-239G>T
ENST00000647353.1:n.54-10461G>T
ENST00000651471.1:n.134-239G>T
ENST00000679909.1:c.28+13549G>T	ENSP00000506089.1:n.28+13549G>T
ENST00000453660.3:n.111-239G>T
ENST00000538324.2:c.99-239G>T	ENSP00000483018.1:n.99-239G>T
ENST00000611156.4:c.99-239G>T	ENSP00000483265.1:n.99-239G>T
NM_020469.2:c.99-239G>T	NP_065202.2:n.99-239G>T
NM_020469.3:c.99-239G>T	NP_065202.2:n.99-239G>T