Canonical Allele Identifier: CA15351035
Gene: LINC01182 HGNC NCBI

Linked Data

dbSNP Id: rs10805321
gnomAD v2: 4-13914373-C-A
gnomAD v3: 4-13912749-C-A
gnomAD v4: 4-13912749-C-A

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