Canonical Allele Identifier: CA1422921633
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573915C= , CM000665.2:g.177573915C= GRCh38
NC_000003.11:g.177291703C= , CM000665.1:g.177291703C= GRCh37
NC_000003.10:g.178774397C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_047568.1:n.289+34422C=
XR_924737.1:n.114-2549G=