Canonical Allele Identifier: CA12642189

Gene: LINC01162

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954872A>G , CM000669.2:g.20954872A>G	GRCh38
NC_000007.13:g.20994491A>G , CM000669.1:g.20994491A>G	GRCh37
NC_000007.12:g.20961016A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.152-65996A>G