Canonical Allele Identifier: CA846003657

Gene: LINC00208

Linked Data

• dbSNP Id: rs1234356936
• MyVariant Identifiers: chr8:g.11435340T>A (hg19) ; chr8:g.11577831T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577831T>A , CM000670.2:g.11577831T>A	GRCh38
NC_000008.10:g.11435340T>A , CM000670.1:g.11435340T>A	GRCh37
NC_000008.9:g.11472749T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.783+514T>A