Canonical Allele Identifier: CA1882581016
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256362A= , CM000671.2:g.133256362A= GRCh38
NC_000009.11:g.136131749A= , CM000671.1:g.136131749A= GRCh37
NC_000009.10:g.135121570A= NCBI36
NG_006669.1:g.21306T=
NG_006669.2:g.23854T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-6T=
ENST00000647353.1:n.54-5210T=
ENST00000651471.1:n.330-6T=
ENST00000679909.1:c.28+18800T= ENSP00000506089.1:n.28+18800T=
ENST00000453660.3:n.386-6T=
ENST00000538324.2:c.372-6T= ENSP00000483018.1:n.372-6T=
ENST00000611156.4:c.372-6T= ENSP00000483265.1:n.372-6T=
NM_020469.2:c.375-6T= NP_065202.2:n.375-6T=
NM_020469.3:c.375-6T= NP_065202.2:n.375-6T=