Canonical Allele Identifier: CA1422921607
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573851C= , CM000665.2:g.177573851C= GRCh38
NC_000003.11:g.177291639C= , CM000665.1:g.177291639C= GRCh37
NC_000003.10:g.178774333C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047568.1:n.289+34358C=
XR_924737.1:n.114-2485G=