Canonical Allele Identifier: CA172383955

Gene: LINC00208

Linked Data

• dbSNP Id: rs979408476
• gnomAD v2: 8-11435339-C-G
• gnomAD v3: 8-11577830-C-G
• gnomAD v4: 8-11577830-C-G
• MyVariant Identifiers: chr8:g.11435339C>G (hg19) ; chr8:g.11577830C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577830C>G , CM000670.2:g.11577830C>G	GRCh38
NC_000008.10:g.11435339C>G , CM000670.1:g.11435339C>G	GRCh37
NC_000008.9:g.11472748C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.783+513C>G