Canonical Allele Identifier: CA562420254

Gene: LINC02208

Linked Data

• dbSNP Id: rs1310216082
• gnomAD v2: 5-117701375-G-A
• gnomAD v3: 5-118365680-G-A
• gnomAD v4: 5-118365680-G-A
• MyVariant Identifiers: chr5:g.117701375G>A (hg19) ; chr5:g.118365680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.118365680G>A , CM000667.2:g.118365680G>A	GRCh38
NC_000005.9:g.117701375G>A , CM000667.1:g.117701375G>A	GRCh37
NC_000005.8:g.117729274G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104610.1:n.2658-14173C>T