Canonical Allele Identifier: CA802665965

Gene: LINC02208

Linked Data

• dbSNP Id: rs1344224534
• gnomAD v3: 5-118365681-G-T
• gnomAD v4: 5-118365681-G-T
• MyVariant Identifiers: chr5:g.117701376G>T (hg19) ; chr5:g.118365681G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.118365681G>T , CM000667.2:g.118365681G>T	GRCh38
NC_000005.9:g.117701376G>T , CM000667.1:g.117701376G>T	GRCh37
NC_000005.8:g.117729275G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104610.1:n.2658-14174C>A