Canonical Allele Identifier: CA709662564
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1397994548

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021271dup , CM000676.2:g.88021271dup GRCh38
NC_000014.8:g.88487615dup , CM000676.1:g.88487615dup GRCh37
NC_000014.7:g.87557368dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2407dup