Canonical Allele Identifier: CA1056770906
Gene: LINC00578 HGNC NCBI

Linked Data

dbSNP Id: rs966005591

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573837A>C , CM000665.2:g.177573837A>C GRCh38
NC_000003.11:g.177291625A>C , CM000665.1:g.177291625A>C GRCh37
NC_000003.10:g.178774319A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047568.1:n.289+34344A>C
XR_924737.1:n.114-2471T>G