Canonical Allele Identifier: CA1439879367
Gene: LINC01182 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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