Canonical Allele Identifier: CA802666099

Gene: LINC02208

Linked Data

• dbSNP Id: rs1260618197
• gnomAD v3: 5-118365871-A-C
• gnomAD v4: 5-118365871-A-C
• MyVariant Identifiers: chr5:g.117701566A>C (hg19) ; chr5:g.118365871A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.118365871A>C , CM000667.2:g.118365871A>C	GRCh38
NC_000005.9:g.117701566A>C , CM000667.1:g.117701566A>C	GRCh37
NC_000005.8:g.117729465A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104610.1:n.2658-14364T>G