Canonical Allele Identifier: CA1882583441
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258378C= , CM000671.2:g.133258378C= GRCh38
NC_000009.11:g.136133769C= , CM000671.1:g.136133769C= GRCh37
NC_000009.10:g.135123590C= NCBI36
NG_006669.1:g.19285G=
NG_006669.2:g.21837G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-246G=
ENST00000647353.1:n.54-7226G=
ENST00000651471.1:n.239-246G=
ENST00000679909.1:c.28+16784G= ENSP00000506089.1:n.28+16784G=
ENST00000453660.3:n.216-246G=
ENST00000538324.2:c.204-246G= ENSP00000483018.1:n.204-246G=
ENST00000611156.4:c.204-246G= ENSP00000483265.1:n.204-246G=
NM_020469.2:c.204-246G= NP_065202.2:n.204-246G=
NM_020469.3:c.204-246G= NP_065202.2:n.204-246G=