Canonical Allele Identifier: CA212132

Gene: LINC02208

Linked Data

• ClinVar Variation Id: 156995
• ClinVar RCV Id: RCV000161421
• MyVariant Identifiers: chr5:g.117701468_117707373del (hg19) ; chr5:g.118365773_118371678del (hg38)
• PubMed: PMID:25666259

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.118365774_118371679del , CM000667.2:g.118365774_118371679del	GRCh38
NC_000005.9:g.117701469_117707374del , CM000667.1:g.117701469_117707374del	GRCh37
NC_000005.8:g.117729368_117735273del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_104610.1:n.2658-20170_2658-14265del