Canonical Allele Identifier: CA1763972922
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802028557

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577988_11577989insA , CM000670.2:g.11577988_11577989insA GRCh38
NC_000008.10:g.11435497_11435498insA , CM000670.1:g.11435497_11435498insA GRCh37
NC_000008.9:g.11472906_11472907insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-382_784-381insA