Canonical Allele Identifier: CA914271956
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs1568137735

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209765T>C , CM000680.2:g.64209765T>C GRCh38
NC_000018.9:g.61877000T>C , CM000680.1:g.61877000T>C GRCh37
NC_000018.8:g.60027980T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39536T>C