Canonical Allele Identifier: CA2309139632
Gene: LINC01924 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209916A= , CM000680.2:g.64209916A= GRCh38
NC_000018.9:g.61877151A= , CM000680.1:g.61877151A= GRCh37
NC_000018.8:g.60028131A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39385A=