Canonical Allele Identifier: CA802666062

Gene: LINC02208

Linked Data

• dbSNP Id: rs1257068024
• MyVariant Identifiers: chr5:g.117701491del (hg19) ; chr5:g.118365796del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.118365796del , CM000667.2:g.118365796del	GRCh38
NC_000005.9:g.117701491del , CM000667.1:g.117701491del	GRCh37
NC_000005.8:g.117729390del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104610.1:n.2658-14289del