Canonical Allele Identifier: CA2733995592
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs2143093770

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854676G>C , CM000679.2:g.69854676G>C GRCh38
NC_000017.10:g.67850817G>C , CM000679.1:g.67850817G>C GRCh37
NC_000017.9:g.65362412G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9190G>C
NR_109972.1:n.363+9190G>C