Canonical Allele Identifier: CA846003682

Gene: LINC00208

Linked Data

• dbSNP Id: rs1210434643
• gnomAD v3: 8-11577884-C-T
• gnomAD v4: 8-11577884-C-T
• MyVariant Identifiers: chr8:g.11435393C>T (hg19) ; chr8:g.11577884C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577884C>T , CM000670.2:g.11577884C>T	GRCh38
NC_000008.10:g.11435393C>T , CM000670.1:g.11435393C>T	GRCh37
NC_000008.9:g.11472802C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-486C>T