Canonical Allele Identifier: CA846003707

Gene: LINC00208

Linked Data

• dbSNP Id: rs1371388135
• gnomAD v3: 8-11577930-T-A
• gnomAD v4: 8-11577930-T-A
• MyVariant Identifiers: chr8:g.11435439T>A (hg19) ; chr8:g.11577930T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577930T>A , CM000670.2:g.11577930T>A	GRCh38
NC_000008.10:g.11435439T>A , CM000670.1:g.11435439T>A	GRCh37
NC_000008.9:g.11472848T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040035.1:n.784-440T>A