Canonical Allele Identifier: CA580018059

Gene: LINC00208

Linked Data

• dbSNP Id: rs1310614142
• gnomAD v2: 8-11435422-A-G
• gnomAD v3: 8-11577913-A-G
• gnomAD v4: 8-11577913-A-G
• MyVariant Identifiers: chr8:g.11435422A>G (hg19) ; chr8:g.11577913A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577913A>G , CM000670.2:g.11577913A>G	GRCh38
NC_000008.10:g.11435422A>G , CM000670.1:g.11435422A>G	GRCh37
NC_000008.9:g.11472831A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040035.1:n.784-457A>G