Canonical Allele Identifier: CA172383960

Gene: LINC00208

Linked Data

• dbSNP Id: rs897410423
• MyVariant Identifiers: chr8:g.11435389C>T (hg19) ; chr8:g.11577880C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577880C>T , CM000670.2:g.11577880C>T	GRCh38
NC_000008.10:g.11435389C>T , CM000670.1:g.11435389C>T	GRCh37
NC_000008.9:g.11472798C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-490C>T