Canonical Allele Identifier: CA2581333769
Community Standard Title: NC_000018.10:g.6567183A>T
Gene: LINC01387 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.6567183A>T , CM000680.2:g.6567183A>T GRCh38
NC_000018.9:g.6567182A>T , CM000680.1:g.6567182A>T GRCh37
NC_000018.8:g.6557182A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120518.1:n.284-8807A>T
XR_001753341.2:n.1022A>T
XR_935116.1:n.98-1350A>T
XR_935116.3:n.365-1350A>T