Canonical Allele Identifier: CA709662500
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1177058599

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021186G>C , CM000676.2:g.88021186G>C GRCh38
NC_000014.8:g.88487530G>C , CM000676.1:g.88487530G>C GRCh37
NC_000014.7:g.87557283G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.328-2483C>G