Canonical Allele Identifier: CA2842464927
Gene: LINC01153 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179813T>G , CM000672.2:g.121179813T>G GRCh38
NC_000010.10:g.122939327T>G , CM000672.1:g.122939327T>G GRCh37
NC_000010.9:g.122929317T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+841T>G