Canonical Allele Identifier: CA1422921631
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573911G= , CM000665.2:g.177573911G= GRCh38
NC_000003.11:g.177291699G= , CM000665.1:g.177291699G= GRCh37
NC_000003.10:g.178774393G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_047568.1:n.289+34418G=
XR_924737.1:n.114-2545C=