Canonical Allele Identifier: CA1422921598
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573830T= , CM000665.2:g.177573830T= GRCh38
NC_000003.11:g.177291618T= , CM000665.1:g.177291618T= GRCh37
NC_000003.10:g.178774312T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047568.1:n.289+34337T=
XR_924737.1:n.114-2464A=