Canonical Allele Identifier: CA770634297

Gene: LINC01122

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.58606358A>T , CM000664.2:g.58606358A>T	GRCh38
NC_000002.11:g.58833493A>T , CM000664.1:g.58833493A>T	GRCh37
NC_000002.10:g.58686997A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033873.1:n.186-50292A>T