Canonical Allele Identifier: CA243588792

Gene: LINC02356

Linked Data

• dbSNP Id: rs753232979
• MyVariant Identifiers: chr12:g.111836626C>T (hg19) ; chr12:g.111398822C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398822C>T , CM000674.2:g.111398822C>T	GRCh38
NC_000012.11:g.111836626C>T , CM000674.1:g.111836626C>T	GRCh37
NC_000012.10:g.110321009C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+1949C>T