Canonical Allele Identifier: CA1763972881
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802027096

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577923del , CM000670.2:g.11577923del GRCh38
NC_000008.10:g.11435432del , CM000670.1:g.11435432del GRCh37
NC_000008.9:g.11472841del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-447del