Canonical Allele Identifier: CA1763972873
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802026808

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577910del , CM000670.2:g.11577910del GRCh38
NC_000008.10:g.11435419del , CM000670.1:g.11435419del GRCh37
NC_000008.9:g.11472828del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-460del