Canonical Allele Identifier: CA2272849587
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854486C= , CM000679.2:g.69854486C= GRCh38
NC_000017.10:g.67850627C= , CM000679.1:g.67850627C= GRCh37
NC_000017.9:g.65362222C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9000C=
NR_109972.1:n.363+9000C=