Canonical Allele Identifier: CA2692331617
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133262067C>A , CM000671.2:g.133262067C>A GRCh38
NC_000009.11:g.136137470C>A , CM000671.1:g.136137470C>A GRCh37
NC_000009.10:g.135127291C>A NCBI36
NG_006669.1:g.15582G>T
NG_006669.2:g.18148G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+32G>T
ENST00000647353.1:n.54-10915G>T
ENST00000651471.1:n.133+32G>T
ENST00000679909.1:c.28+13095G>T ENSP00000506089.1:n.28+13095G>T
ENST00000453660.3:n.110+32G>T
ENST00000538324.2:c.98+32G>T ENSP00000483018.1:n.98+32G>T
ENST00000611156.4:c.98+32G>T ENSP00000483265.1:n.98+32G>T
NM_020469.2:c.98+32G>T NP_065202.2:n.98+32G>T
NM_020469.3:c.98+32G>T NP_065202.2:n.98+32G>T