Canonical Allele Identifier: CA13643677

Gene: LINC02398

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20077705A>G , CM000674.2:g.20077705A>G	GRCh38
NC_000012.11:g.20230639A>G , CM000674.1:g.20230639A>G	GRCh37
NC_000012.10:g.20121906A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040098.1:n.410-21047A>G