Canonical Allele Identifier: CA2580597883
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258352C>A , CM000671.2:g.133258352C>A GRCh38
NG_006669.1:g.19311G>T
NG_006669.2:g.21863G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-220G>T
ENST00000647353.1:n.54-7200G>T
ENST00000651471.1:n.239-220G>T
ENST00000679909.1:c.28+16810G>T ENSP00000506089.1:n.28+16810G>T
ENST00000453660.3:n.216-220G>T
ENST00000538324.2:c.204-220G>T ENSP00000483018.1:n.204-220G>T
ENST00000611156.4:c.204-220G>T ENSP00000483265.1:n.204-220G>T
NM_020469.2:c.204-220G>T NP_065202.2:n.204-220G>T
NM_020469.3:c.204-220G>T NP_065202.2:n.204-220G>T