Canonical Allele Identifier: CA991159735
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs1599264082

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209782G>T , CM000680.2:g.64209782G>T GRCh38
NC_000018.9:g.61877017G>T , CM000680.1:g.61877017G>T GRCh37
NC_000018.8:g.60027997G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39519G>T