Canonical Allele Identifier: CA2309139640
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs2051786694

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209924C>T , CM000680.2:g.64209924C>T GRCh38
NC_000018.9:g.61877159C>T , CM000680.1:g.61877159C>T GRCh37
NC_000018.8:g.60028139C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39377C>T