Canonical Allele Identifier: CA321892229

Gene: LINC00163

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44993730A>G , CM000683.2:g.44993730A>G	GRCh38
NC_000021.8:g.46413645A>G , CM000683.1:g.46413645A>G	GRCh37
NC_000021.7:g.45238073A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033840.1:n.183+174T>C