Canonical Allele Identifier: CA1763972950
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1319178263

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578048C>A , CM000670.2:g.11578048C>A GRCh38
NC_000008.10:g.11435557C>A , CM000670.1:g.11435557C>A GRCh37
NC_000008.9:g.11472966C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-322C>A