Canonical Allele Identifier: CA846003696

Gene: LINC00208

Linked Data

• dbSNP Id: rs1390476891
• gnomAD v3: 8-11577919-C-A
• gnomAD v4: 8-11577919-C-A
• MyVariant Identifiers: chr8:g.11435428C>A (hg19) ; chr8:g.11577919C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577919C>A , CM000670.2:g.11577919C>A	GRCh38
NC_000008.10:g.11435428C>A , CM000670.1:g.11435428C>A	GRCh37
NC_000008.9:g.11472837C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040035.1:n.784-451C>A