Canonical Allele Identifier: CA1763972927

Gene: LINC00208

Linked Data

• dbSNP Id: rs967720208

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577997C>A , CM000670.2:g.11577997C>A	GRCh38
NC_000008.10:g.11435506C>A , CM000670.1:g.11435506C>A	GRCh37
NC_000008.9:g.11472915C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-373C>A