Canonical Allele Identifier: CA903067206
Gene: LINC00578 HGNC NCBI

Linked Data

dbSNP Id: rs1195386946

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.177573865G>A , CM000665.2:g.177573865G>A GRCh38
NC_000003.11:g.177291653G>A , CM000665.1:g.177291653G>A GRCh37
NC_000003.10:g.178774347G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_047568.1:n.289+34372G>A
XR_924737.1:n.114-2499C>T