Canonical Allele Identifier: CA348289981
Gene: IL36RN HGNC NCBI

Linked Data

ClinVar Variation Id: 1052879
ClinVar RCV Id: RCV001361143
dbSNP Id: rs1685654399
gnomAD v3: 2-113062147-A-G
gnomAD v4: 2-113062147-A-G
MyVariant Identifiers: chr2:g.113819724A>G (hg19) chr2:g.113062147A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062147A>G , CM000664.2:g.113062147A>G GRCh38
NC_000002.11:g.113819724A>G , CM000664.1:g.113819724A>G GRCh37
NC_000002.10:g.113536195A>G NCBI36
NG_031864.1:g.8510A>G , LRG_730:g.8510A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.139A>G ENSP00000409262.2:p.Asn47Asp
ENST00000393200.7:c.139A>G MANE Select ENSP00000376896.2:p.Asn47Asp
ENST00000346807.7:c.139A>G ENSP00000259212.3:p.Asn47Asp
ENST00000393200.6:c.139A>G ENSP00000376896.2:p.Asn47Asp
ENST00000437409.1:c.139A>G ENSP00000409262.1:p.Asn47Asp
NM_012275.2:c.139A>G , LRG_730t2:c.139A>G NP_036407.1:p.Asn47Asp
NM_173170.1:c.139A>G , LRG_730t1:c.139A>G NP_775262.1:p.Asn47Asp
NM_012275.3:c.139A>G MANE Select NP_036407.1:p.Asn47Asp
Search 100 bp 5'
Search 100 bp 3'