Canonical Allele Identifier: CA1838443
Gene: IL36RN HGNC NCBI

Linked Data

ClinVar Variation Id: 2579641
ClinVar RCV Id: RCV003328076
dbSNP Id: rs144478519
ExAC: 2:113820124 C / A
gnomAD v2: 2-113820124-C-A
gnomAD v4: 2-113062547-C-A
MyVariant Identifiers: chr2:g.113820124C>A (hg19) chr2:g.113062547C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062547C>A , CM000664.2:g.113062547C>A GRCh38
NC_000002.11:g.113820124C>A , CM000664.1:g.113820124C>A GRCh37
NC_000002.10:g.113536595C>A NCBI36
NG_031864.1:g.8910C>A , LRG_730:g.8910C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000437409.2:c.338C>A ENSP00000409262.2:p.Ser113Ter
ENST00000393200.7:c.338C>A MANE Select ENSP00000376896.2:p.Ser113Ter
ENST00000346807.7:c.338C>A ENSP00000259212.3:p.Ser113Ter
ENST00000393200.6:c.338C>A ENSP00000376896.2:p.Ser113Ter
ENST00000437409.1:c.338C>A ENSP00000409262.1:p.Ser113Ter
ENST00000514072.1:c.28C>A
NM_012275.2:c.338C>A , LRG_730t2:c.338C>A NP_036407.1:p.Ser113Ter
NM_173170.1:c.338C>A , LRG_730t1:c.338C>A NP_775262.1:p.Ser113Ter
NM_012275.3:c.338C>A MANE Select NP_036407.1:p.Ser113Ter
Search 100 bp 5'
Search 100 bp 3'