Canonical Allele Identifier: CA1576425887
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1753181706

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14334del