Canonical Allele Identifier: CA15351035

Gene: LINC01182

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.13912749C>A , CM000666.2:g.13912749C>A	GRCh38
NC_000004.11:g.13914373C>A , CM000666.1:g.13914373C>A	GRCh37
NC_000004.10:g.13523471C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121681.1:n.350-16601C>A
XR_001741379.1:n.5109-18795C>A
XR_001741381.2:n.5108+74290C>A