Canonical Allele Identifier: CA13637048

Gene: LINC02375

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.127329196G>A , CM000674.2:g.127329196G>A	GRCh38
NC_000012.11:g.127813741G>A , CM000674.1:g.127813741G>A	GRCh37
NC_000012.10:g.126379694G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110057.1:n.202-4391C>T