Canonical Allele Identifier: CA2309139641
Gene: LINC01924 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209925T= , CM000680.2:g.64209925T= GRCh38
NC_000018.9:g.61877160T= , CM000680.1:g.61877160T= GRCh37
NC_000018.8:g.60028140T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39376T=