Canonical Allele Identifier: CA1280039538
Gene: IL36RN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060847T= , CM000664.2:g.113060847T= GRCh38
NC_000002.11:g.113818424T= , CM000664.1:g.113818424T= GRCh37
NC_000002.10:g.113534895T= NCBI36
NG_031864.1:g.7210T= , LRG_730:g.7210T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.30-5T= ENSP00000409262.2:n.30-5T=
ENST00000393200.7:c.30-5T= MANE Select ENSP00000376896.2:n.30-5T=
ENST00000346807.7:c.30-5T= ENSP00000259212.3:n.30-5T=
ENST00000393200.6:c.30-5T= ENSP00000376896.2:n.30-5T=
ENST00000437409.1:c.30-5T= ENSP00000409262.1:n.30-5T=
NM_012275.2:c.30-5T= , LRG_730t2:c.30-5T= NP_036407.1:n.30-5T=
NM_173170.1:c.30-5T= , LRG_730t1:c.30-5T= NP_775262.1:n.30-5T=
NM_012275.3:c.30-5T= MANE Select NP_036407.1:n.30-5T=
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