Canonical Allele Identifier: CA172383969

Gene: LINC00208

Linked Data

• dbSNP Id: rs1007011809
• MyVariant Identifiers: chr8:g.11435410G>C (hg19) ; chr8:g.11577901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577901G>C , CM000670.2:g.11577901G>C	GRCh38
NC_000008.10:g.11435410G>C , CM000670.1:g.11435410G>C	GRCh37
NC_000008.9:g.11472819G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-469G>C