Canonical Allele Identifier: CA1422921608
Gene: LINC00578 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573852T= , CM000665.2:g.177573852T= GRCh38
NC_000003.11:g.177291640T= , CM000665.1:g.177291640T= GRCh37
NC_000003.10:g.178774334T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047568.1:n.289+34359T=
XR_924737.1:n.114-2486A=