Canonical Allele Identifier: CA846003576

Gene: LINC00208

Linked Data

• dbSNP Id: rs1183632836
• MyVariant Identifiers: chr8:g.11435251C>G (hg19) ; chr8:g.11577742C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577742C>G , CM000670.2:g.11577742C>G	GRCh38
NC_000008.10:g.11435251C>G , CM000670.1:g.11435251C>G	GRCh37
NC_000008.9:g.11472660C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.783+425C>G