Canonical Allele Identifier: CA2573133157
Gene: IL36RN HGNC NCBI

Linked Data

ClinVar Variation Id: 1648636
ClinVar RCV Id: RCV002141290
dbSNP Id: rs2105069464
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062267T>C , CM000664.2:g.113062267T>C GRCh38
NC_000002.11:g.113819844T>C , CM000664.1:g.113819844T>C GRCh37
NC_000002.10:g.113536315T>C NCBI36
NG_031864.1:g.8630T>C , LRG_730:g.8630T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.243+16T>C ENSP00000409262.2:n.243+16T>C
ENST00000393200.7:c.243+16T>C MANE Select ENSP00000376896.2:n.243+16T>C
ENST00000346807.7:c.243+16T>C ENSP00000259212.3:n.243+16T>C
ENST00000393200.6:c.243+16T>C ENSP00000376896.2:n.243+16T>C
ENST00000437409.1:c.243+16T>C ENSP00000409262.1:n.243+16T>C
NM_012275.2:c.243+16T>C , LRG_730t2:c.243+16T>C NP_036407.1:n.243+16T>C
NM_173170.1:c.243+16T>C , LRG_730t1:c.243+16T>C NP_775262.1:n.243+16T>C
NM_012275.3:c.243+16T>C MANE Select NP_036407.1:n.243+16T>C
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