Canonical Allele Identifier: CA1882581290
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256487G= , CM000671.2:g.133256487G= GRCh38
NC_000009.11:g.136131874G= , CM000671.1:g.136131874G= GRCh37
NC_000009.10:g.135121695G= NCBI36
NG_006669.1:g.21181C=
NG_006669.2:g.23729C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-131C=
ENST00000647353.1:n.54-5335C=
ENST00000651471.1:n.330-131C=
ENST00000679909.1:c.28+18675C= ENSP00000506089.1:n.28+18675C=
ENST00000453660.3:n.386-131C=
ENST00000538324.2:c.372-131C= ENSP00000483018.1:n.372-131C=
ENST00000611156.4:c.372-131C= ENSP00000483265.1:n.372-131C=
NM_020469.2:c.375-131C= NP_065202.2:n.375-131C=
NM_020469.3:c.375-131C= NP_065202.2:n.375-131C=