Canonical Allele Identifier: CA933228072
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs998748565

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179915A>G , CM000672.2:g.121179915A>G GRCh38
NC_000010.10:g.122939429A>G , CM000672.1:g.122939429A>G GRCh37
NC_000010.9:g.122929419A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+943A>G