Canonical Allele Identifier: CA562420278

Gene: LINC02208

Linked Data

• dbSNP Id: rs1225115375
• gnomAD v2: 5-117701537-A-G
• gnomAD v3: 5-118365842-A-G
• gnomAD v4: 5-118365842-A-G
• MyVariant Identifiers: chr5:g.117701537A>G (hg19) ; chr5:g.118365842A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.118365842A>G , CM000667.2:g.118365842A>G	GRCh38
NC_000005.9:g.117701537A>G , CM000667.1:g.117701537A>G	GRCh37
NC_000005.8:g.117729436A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104610.1:n.2658-14335T>C