Canonical Allele Identifier: CA2789745613
Gene: LINC01153 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179908_121179911dup , CM000672.2:g.121179908_121179911dup GRCh38
NC_000010.10:g.122939422_122939425dup , CM000672.1:g.122939422_122939425dup GRCh37
NC_000010.9:g.122929412_122929415dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+936_684+939dup