Canonical Allele Identifier: CA348289132
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs1685627126
COSMIC: COSM1751997
MyVariant Identifiers: chr2:g.113818428G>A (hg19) chr2:g.113060851G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060851G>A , CM000664.2:g.113060851G>A GRCh38
NC_000002.11:g.113818428G>A , CM000664.1:g.113818428G>A GRCh37
NC_000002.10:g.113534899G>A NCBI36
NG_031864.1:g.7214G>A , LRG_730:g.7214G>A

Transcript Alleles

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