Canonical Allele Identifier: CA1882584337
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834679471

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260052_133260055dup , CM000671.2:g.133260052_133260055dup GRCh38
NC_000009.11:g.136135456_136135459dup , CM000671.1:g.136135456_136135459dup GRCh37
NC_000009.10:g.135125277_135125280dup NCBI36
NG_006669.1:g.17595_17598dup
NG_006669.2:g.20160_20163dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-189_186-186dup
ENST00000647353.1:n.54-8903_54-8900dup
ENST00000651471.1:n.191-189_191-186dup
ENST00000679909.1:c.28+15107_28+15110dup ENSP00000506089.1:n.28+15107_28+15110dup
ENST00000453660.3:n.168-189_168-186dup
ENST00000538324.2:c.156-189_156-186dup ENSP00000483018.1:n.156-189_156-186dup
ENST00000611156.4:c.156-189_156-186dup ENSP00000483265.1:n.156-189_156-186dup
NM_020469.2:c.156-189_156-186dup NP_065202.2:n.156-189_156-186dup
NM_020469.3:c.156-189_156-186dup NP_065202.2:n.156-189_156-186dup