Canonical Allele Identifier: CA15285004

Gene: LINC00578

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.177586510C>T , CM000665.2:g.177586510C>T	GRCh38
NC_000003.11:g.177304298C>T , CM000665.1:g.177304298C>T	GRCh37
NC_000003.10:g.178786992C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_047568.1:n.290-42907C>T
XR_924737.1:n.113+7730G>A