Canonical Allele Identifier: CA1035134221
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs1685662518
gnomAD v3: 2-113062471-CTCT-C
gnomAD v4: 2-113062471-CTCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062472_113062474del , CM000664.2:g.113062472_113062474del GRCh38
NC_000002.11:g.113820049_113820051del , CM000664.1:g.113820049_113820051del GRCh37
NC_000002.10:g.113536520_113536522del NCBI36
NG_031864.1:g.8835_8837del , LRG_730:g.8835_8837del

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.263_265del ENSP00000409262.2:p.Leu88_Tyr89delinsHis
ENST00000393200.7:c.263_265del MANE Select ENSP00000376896.2:p.Leu88_Tyr89delinsHis
ENST00000346807.7:c.263_265del ENSP00000259212.3:p.Leu88_Tyr89delinsHis
ENST00000393200.6:c.263_265del ENSP00000376896.2:p.Leu88_Tyr89delinsHis
ENST00000437409.1:c.263_265del ENSP00000409262.1:p.Leu88_Tyr89delinsHis
NM_012275.2:c.263_265del , LRG_730t2:c.263_265del NP_036407.1:p.Leu88_Tyr89delinsHis
NM_173170.1:c.263_265del , LRG_730t1:c.263_265del NP_775262.1:p.Leu88_Tyr89delinsHis
NM_012275.3:c.263_265del MANE Select NP_036407.1:p.Leu88_Tyr89delinsHis
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