Canonical Allele Identifier: CA709662498
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1417690524

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021169_88021170dup , CM000676.2:g.88021169_88021170dup GRCh38
NC_000014.8:g.88487513_88487514dup , CM000676.1:g.88487513_88487514dup GRCh37
NC_000014.7:g.87557266_87557267dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.328-2466_328-2465dup