Canonical Allele Identifier: CA2309139594
Gene: LINC01924 HGNC NCBI

Linked Data

dbSNP Id: rs2051786240

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209831A>G , CM000680.2:g.64209831A>G GRCh38
NC_000018.9:g.61877066A>G , CM000680.1:g.61877066A>G GRCh37
NC_000018.8:g.60028046A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39470A>G