Canonical Allele Identifier: CA615660985
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1303027486

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021176G>A , CM000676.2:g.88021176G>A GRCh38
NC_000014.8:g.88487520G>A , CM000676.1:g.88487520G>A GRCh37
NC_000014.7:g.87557273G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.328-2473C>T