Canonical Allele Identifier: CA1940871562
Gene: LINC01153 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179861A= , CM000672.2:g.121179861A= GRCh38
NC_000010.10:g.122939375A= , CM000672.1:g.122939375A= GRCh37
NC_000010.9:g.122929365A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+889A=