Canonical Allele Identifier: CA2272849716
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854772G= , CM000679.2:g.69854772G= GRCh38
NC_000017.10:g.67850913G= , CM000679.1:g.67850913G= GRCh37
NC_000017.9:g.65362508G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9286G=
NR_109972.1:n.363+9286G=