Canonical Allele Identifier: CA2309139605
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs2051786325

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209851T>C , CM000680.2:g.64209851T>C GRCh38
NC_000018.9:g.61877086T>C , CM000680.1:g.61877086T>C GRCh37
NC_000018.8:g.60028066T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39450T>C