Canonical Allele Identifier: CA2581353856
Gene: LINC01924 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209921A>C , CM000680.2:g.64209921A>C GRCh38
NC_000018.9:g.61877156A>C , CM000680.1:g.61877156A>C GRCh37
NC_000018.8:g.60028136A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39380A>C