Canonical Allele Identifier: CA774555019
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1164477365

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9286G>A
NR_109972.1:n.363+9286G>A