Canonical Allele Identifier: CA53688661
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs866442385

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062249G>C , CM000664.2:g.113062249G>C GRCh38
NC_000002.11:g.113819826G>C , CM000664.1:g.113819826G>C GRCh37
NC_000002.10:g.113536297G>C NCBI36
NG_031864.1:g.8612G>C , LRG_730:g.8612G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.241G>C ENSP00000409262.2:p.Glu81Gln
ENST00000393200.7:c.241G>C MANE Select ENSP00000376896.2:p.Glu81Gln
ENST00000346807.7:c.241G>C ENSP00000259212.3:p.Glu81Gln
ENST00000393200.6:c.241G>C ENSP00000376896.2:p.Glu81Gln
ENST00000437409.1:c.241G>C ENSP00000409262.1:p.Glu81Gln
NM_012275.2:c.241G>C , LRG_730t2:c.241G>C NP_036407.1:p.Glu81Gln
NM_173170.1:c.241G>C , LRG_730t1:c.241G>C NP_775262.1:p.Glu81Gln
NM_012275.3:c.241G>C MANE Select NP_036407.1:p.Glu81Gln