Canonical Allele Identifier: CA580017990

Gene: LINC00208

Linked Data

• dbSNP Id: rs1315489641
• gnomAD v2: 8-11435202-C-T
• gnomAD v3: 8-11577693-C-T
• gnomAD v4: 8-11577693-C-T
• MyVariant Identifiers: chr8:g.11435202C>T (hg19) ; chr8:g.11577693C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577693C>T , CM000670.2:g.11577693C>T	GRCh38
NC_000008.10:g.11435202C>T , CM000670.1:g.11435202C>T	GRCh37
NC_000008.9:g.11472611C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.783+376C>T