Canonical Allele Identifier: CA321311313
Gene: LINC01679 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43359800C>T , CM000683.2:g.43359800C>T GRCh38
NC_000021.8:g.44779680C>T , CM000683.1:g.44779680C>T GRCh37
NC_000021.7:g.43604108C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131902.1:n.1459-314G>A
XR_244326.3:n.1205-314G>A