Canonical Allele Identifier: CA1110700037

Gene: LINC00208

Linked Data

• dbSNP Id: rs1802025424
• gnomAD v3: 8-11577857-G-A
• gnomAD v4: 8-11577857-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577857G>A , CM000670.2:g.11577857G>A	GRCh38
NC_000008.10:g.11435366G>A , CM000670.1:g.11435366G>A	GRCh37
NC_000008.9:g.11472775G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-513G>A