Canonical Allele Identifier: CA172383971

Gene: LINC00208

Linked Data

• dbSNP Id: rs780846401
• gnomAD v2: 8-11435421-G-C
• gnomAD v3: 8-11577912-G-C
• gnomAD v4: 8-11577912-G-C
• MyVariant Identifiers: chr8:g.11435421G>C (hg19) ; chr8:g.11577912G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577912G>C , CM000670.2:g.11577912G>C	GRCh38
NC_000008.10:g.11435421G>C , CM000670.1:g.11435421G>C	GRCh37
NC_000008.9:g.11472830G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040035.1:n.784-458G>C