Canonical Allele Identifier: CA2309139626
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs558184821

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209904G>C , CM000680.2:g.64209904G>C GRCh38
NC_000018.9:g.61877139G>C , CM000680.1:g.61877139G>C GRCh37
NC_000018.8:g.60028119G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39397G>C