Canonical Allele Identifier: CA1035134147
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs1685660171
gnomAD v3: 2-113062401-TC-T
gnomAD v4: 2-113062401-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062404del , CM000664.2:g.113062404del GRCh38
NC_000002.11:g.113819981del , CM000664.1:g.113819981del GRCh37
NC_000002.10:g.113536452del NCBI36
NG_031864.1:g.8767del , LRG_730:g.8767del

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.244-49del ENSP00000409262.2:n.244-49del
ENST00000393200.7:c.244-49del MANE Select ENSP00000376896.2:n.244-49del
ENST00000346807.7:c.244-49del ENSP00000259212.3:n.244-49del
ENST00000393200.6:c.244-49del ENSP00000376896.2:n.244-49del
ENST00000437409.1:c.244-49del ENSP00000409262.1:n.244-49del
NM_012275.2:c.244-49del , LRG_730t2:c.244-49del NP_036407.1:n.244-49del
NM_173170.1:c.244-49del , LRG_730t1:c.244-49del NP_775262.1:n.244-49del
NM_012275.3:c.244-49del MANE Select NP_036407.1:n.244-49del
Search 100 bp 5'
Search 100 bp 3'