Canonical Allele Identifier: CA2272849569
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854425C= , CM000679.2:g.69854425C= GRCh38
NC_000017.10:g.67850566C= , CM000679.1:g.67850566C= GRCh37
NC_000017.9:g.65362161C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+8939C=
NR_109972.1:n.363+8939C=