Canonical Allele Identifier: CA2521692996
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260128G>T , CM000671.2:g.133260128G>T GRCh38
NC_000009.11:g.136135532G>T , CM000671.1:g.136135532G>T GRCh37
NC_000009.10:g.135125353G>T NCBI36
NG_006669.1:g.17522C>A
NG_006669.2:g.20087C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-262C>A
ENST00000647353.1:n.54-8976C>A
ENST00000651471.1:n.191-262C>A
ENST00000679909.1:c.28+15034C>A ENSP00000506089.1:n.28+15034C>A
ENST00000453660.3:n.168-262C>A
ENST00000538324.2:c.156-262C>A ENSP00000483018.1:n.156-262C>A
ENST00000611156.4:c.156-262C>A ENSP00000483265.1:n.156-262C>A
NM_020469.2:c.156-262C>A NP_065202.2:n.156-262C>A
NM_020469.3:c.156-262C>A NP_065202.2:n.156-262C>A