Canonical Allele Identifier: CA172383956

Gene: LINC00208

Linked Data

• dbSNP Id: rs895353913
• MyVariant Identifiers: chr8:g.11435345G>A (hg19) ; chr8:g.11577836G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577836G>A , CM000670.2:g.11577836G>A	GRCh38
NC_000008.10:g.11435345G>A , CM000670.1:g.11435345G>A	GRCh37
NC_000008.9:g.11472754G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.783+519G>A