Canonical Allele Identifier: CA129266
Gene: IL36RN HGNC NCBI

Linked Data

ClinVar Variation Id: 30489
ClinVar RCV Id: RCV000023446 RCV001090265 RCV002508133
dbSNP Id: rs387906914
ExAC: 2:113818479 T / C
gnomAD v2: 2-113818479-T-C
gnomAD v3: 2-113060902-T-C
gnomAD v4: 2-113060902-T-C
MyVariant Identifiers: chr2:g.113818479T>C (hg19) chr2:g.113060902T>C (hg38)
PubMed: PMID:21848462
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060902T>C , CM000664.2:g.113060902T>C GRCh38
NC_000002.11:g.113818479T>C , CM000664.1:g.113818479T>C GRCh37
NC_000002.10:g.113534950T>C NCBI36
NG_031864.1:g.7265T>C , LRG_730:g.7265T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000437409.2:c.80T>C ENSP00000409262.2:p.Leu27Pro
ENST00000393200.7:c.80T>C MANE Select ENSP00000376896.2:p.Leu27Pro
ENST00000346807.7:c.80T>C ENSP00000259212.3:p.Leu27Pro
ENST00000393200.6:c.80T>C ENSP00000376896.2:p.Leu27Pro
ENST00000437409.1:c.80T>C ENSP00000409262.1:p.Leu27Pro
NM_012275.2:c.80T>C , LRG_730t2:c.80T>C NP_036407.1:p.Leu27Pro
NM_173170.1:c.80T>C , LRG_730t1:c.80T>C NP_775262.1:p.Leu27Pro
NM_012275.3:c.80T>C MANE Select NP_036407.1:p.Leu27Pro
Search 100 bp 5'
Search 100 bp 3'