Canonical Allele Identifier: CA1882584455
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs575259

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260349A>C , CM000671.2:g.133260349A>C GRCh38
NG_006669.1:g.17301T>G
NG_006669.2:g.19866T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-483T>G
ENST00000647353.1:n.54-9197T>G
ENST00000651471.1:n.191-483T>G
ENST00000679909.1:c.28+14813T>G ENSP00000506089.1:n.28+14813T>G
ENST00000453660.3:n.168-483T>G
ENST00000538324.2:c.156-483T>G ENSP00000483018.1:n.156-483T>G
ENST00000611156.4:c.156-483T>G ENSP00000483265.1:n.156-483T>G
NM_020469.2:c.156-483T>G NP_065202.2:n.156-483T>G
NM_020469.3:c.156-483T>G NP_065202.2:n.156-483T>G