Canonical Allele Identifier: CA16099613

Gene: LINC01122

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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