Canonical Allele Identifier: CA348289180
Gene: IL36RN HGNC NCBI

Linked Data

gnomAD v4: 2-113060863-C-A
MyVariant Identifiers: chr2:g.113818440C>A (hg19) chr2:g.113060863C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060863C>A , CM000664.2:g.113060863C>A GRCh38
NC_000002.11:g.113818440C>A , CM000664.1:g.113818440C>A GRCh37
NC_000002.10:g.113534911C>A NCBI36
NG_031864.1:g.7226C>A , LRG_730:g.7226C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.41C>A ENSP00000409262.2:p.Ser14Ter
ENST00000393200.7:c.41C>A MANE Select ENSP00000376896.2:p.Ser14Ter
ENST00000346807.7:c.41C>A ENSP00000259212.3:p.Ser14Ter
ENST00000393200.6:c.41C>A ENSP00000376896.2:p.Ser14Ter
ENST00000437409.1:c.41C>A ENSP00000409262.1:p.Ser14Ter
NM_012275.2:c.41C>A , LRG_730t2:c.41C>A NP_036407.1:p.Ser14Ter
NM_173170.1:c.41C>A , LRG_730t1:c.41C>A NP_775262.1:p.Ser14Ter
NM_012275.3:c.41C>A MANE Select NP_036407.1:p.Ser14Ter
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