Canonical Allele Identifier: CA2309139620
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs2051786453

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209895C>T , CM000680.2:g.64209895C>T GRCh38
NC_000018.9:g.61877130C>T , CM000680.1:g.61877130C>T GRCh37
NC_000018.8:g.60028110C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39406C>T