Canonical Allele Identifier: CA1763972880
Gene: LINC00208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577921_11577922delinsCT , CM000670.2:g.11577921_11577922delinsCT GRCh38
NC_000008.10:g.11435430_11435431delinsCT , CM000670.1:g.11435430_11435431delinsCT GRCh37
NC_000008.9:g.11472839_11472840delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-449_784-448delinsCT