Canonical Allele Identifier: CA787060393

Gene: LINC02465

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.129810129T>A , CM000666.2:g.129810129T>A	GRCh38
NC_000004.11:g.130731284T>A , CM000666.1:g.130731284T>A	GRCh37
NC_000004.10:g.130950734T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_151713.1:n.429-1873T>A