Canonical Allele Identifier: CA1940871586
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs1850761429

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179945dup , CM000672.2:g.121179945dup GRCh38
NC_000010.10:g.122939459dup , CM000672.1:g.122939459dup GRCh37
NC_000010.9:g.122929449dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+973dup