Canonical Allele Identifier: CA89215130
Gene: LINC00578 HGNC NCBI

Linked Data

dbSNP Id: rs1036061952

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573975G>A , CM000665.2:g.177573975G>A GRCh38
NC_000003.11:g.177291763G>A , CM000665.1:g.177291763G>A GRCh37
NC_000003.10:g.178774457G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047568.1:n.289+34482G>A
XR_924737.1:n.114-2609C>T