Canonical Allele Identifier: CA2529778320
Gene: LINC01153 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179887C>A , CM000672.2:g.121179887C>A GRCh38
NC_000010.10:g.122939401C>A , CM000672.1:g.122939401C>A GRCh37
NC_000010.9:g.122929391C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+915C>A