Canonical Allele Identifier: CA172383977

Gene: LINC00208

Linked Data

• dbSNP Id: rs142069021
• gnomAD v2: 8-11435464-G-A
• gnomAD v3: 8-11577955-G-A
• gnomAD v4: 8-11577955-G-A
• MyVariant Identifiers: chr8:g.11435464G>A (hg19) ; chr8:g.11577955G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577955G>A , CM000670.2:g.11577955G>A	GRCh38
NC_000008.10:g.11435464G>A , CM000670.1:g.11435464G>A	GRCh37
NC_000008.9:g.11472873G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-415G>A