Canonical Allele Identifier: CA951840616
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs925892269

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398972C>G , CM000674.2:g.111398972C>G GRCh38
NC_000012.11:g.111836776C>G , CM000674.1:g.111836776C>G GRCh37
NC_000012.10:g.110321159C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2099C>G