Canonical Allele Identifier: CA299724770

Gene: LINC01478

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.44510702C>T , CM000680.2:g.44510702C>T	GRCh38
NC_000018.9:g.42090667C>T , CM000680.1:g.42090667C>T	GRCh37
NC_000018.8:g.40344665C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110792.1:n.386+7523G>A