Canonical Allele Identifier: CA2272849777
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1917510678

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854915C>A , CM000679.2:g.69854915C>A GRCh38
NC_000017.10:g.67851056C>A , CM000679.1:g.67851056C>A GRCh37
NC_000017.9:g.65362651C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9429C>A
NR_109972.1:n.363+9429C>A