Canonical Allele Identifier: CA2759551666
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573946G>A , CM000665.2:g.177573946G>A GRCh38
NC_000003.11:g.177291734G>A , CM000665.1:g.177291734G>A GRCh37
NC_000003.10:g.178774428G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_047568.1:n.289+34453G>A
XR_924737.1:n.114-2580C>T