Canonical Allele Identifier: CA1882580637
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256204C= , CM000671.2:g.133256204C= GRCh38
NC_000009.11:g.136131591C= , CM000671.1:g.136131591C= GRCh37
NC_000009.10:g.135121412C= NCBI36
NG_006669.1:g.21464G=
NG_006669.2:g.24012G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.556G=
ENST00000647353.1:n.54-5052G=
ENST00000651471.1:n.482G=
ENST00000679909.1:c.28+18958G= ENSP00000506089.1:n.28+18958G=
ENST00000453660.3:n.538G=
ENST00000538324.2:c.524G= ENSP00000483018.1:p.Arg175=
ENST00000611156.4:c.524G= ENSP00000483265.1:p.Arg175=
NM_020469.2:c.527G= NP_065202.2:p.Arg176=
NM_020469.3:c.527G= NP_065202.2:p.Arg176=