Canonical Allele Identifier: CA1940871541
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs1850760561

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179837T>A , CM000672.2:g.121179837T>A GRCh38
NC_000010.10:g.122939351T>A , CM000672.1:g.122939351T>A GRCh37
NC_000010.9:g.122929341T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+865T>A