Canonical Allele Identifier: CA1838327
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs763738892
ExAC: 2:113818386 AC / A
MyVariant Identifiers: chr2:g.113818387del (hg19) chr2:g.113060810del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060812del , CM000664.2:g.113060812del GRCh38
NC_000002.11:g.113818389del , CM000664.1:g.113818389del GRCh37
NC_000002.10:g.113534860del NCBI36
NG_031864.1:g.7175del , LRG_730:g.7175del

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.30-40del ENSP00000409262.2:n.30-40del
ENST00000393200.7:c.30-40del MANE Select ENSP00000376896.2:n.30-40del
ENST00000346807.7:c.30-40del ENSP00000259212.3:n.30-40del
ENST00000393200.6:c.30-40del ENSP00000376896.2:n.30-40del
ENST00000437409.1:c.30-40del ENSP00000409262.1:n.30-40del
NM_012275.2:c.30-40del , LRG_730t2:c.30-40del NP_036407.1:n.30-40del
NM_173170.1:c.30-40del , LRG_730t1:c.30-40del NP_775262.1:n.30-40del
NM_012275.3:c.30-40del MANE Select NP_036407.1:n.30-40del
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