Canonical Allele Identifier: CA1422928217
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177586510C>A , CM000665.2:g.177586510C>A GRCh38
NC_000003.11:g.177304298C>A , CM000665.1:g.177304298C>A GRCh37
NC_000003.10:g.178786992C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047568.1:n.290-42907C>A
XR_924737.1:n.113+7730G>T