Canonical Allele Identifier: CA1940871574
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs1850761230

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179905G>T , CM000672.2:g.121179905G>T GRCh38
NC_000010.10:g.122939419G>T , CM000672.1:g.122939419G>T GRCh37
NC_000010.9:g.122929409G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+933G>T