Canonical Allele Identifier: CA232716674

Gene: LINC02367

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9394366T>C , CM000674.2:g.9394366T>C	GRCh38
NC_000012.11:g.9546962T>C , CM000674.1:g.9546962T>C	GRCh37
NC_000012.10:g.9438229T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120479.1:n.2363-165T>C