Canonical Allele Identifier: CA348289142
Gene: IL36RN HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113818431T>C (hg19) chr2:g.113060854T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060854T>C , CM000664.2:g.113060854T>C GRCh38
NC_000002.11:g.113818431T>C , CM000664.1:g.113818431T>C GRCh37
NC_000002.10:g.113534902T>C NCBI36
NG_031864.1:g.7217T>C , LRG_730:g.7217T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.32T>C ENSP00000409262.2:p.Met11Thr
ENST00000393200.7:c.32T>C MANE Select ENSP00000376896.2:p.Met11Thr
ENST00000346807.7:c.32T>C ENSP00000259212.3:p.Met11Thr
ENST00000393200.6:c.32T>C ENSP00000376896.2:p.Met11Thr
ENST00000437409.1:c.32T>C ENSP00000409262.1:p.Met11Thr
NM_012275.2:c.32T>C , LRG_730t2:c.32T>C NP_036407.1:p.Met11Thr
NM_173170.1:c.32T>C , LRG_730t1:c.32T>C NP_775262.1:p.Met11Thr
NM_012275.3:c.32T>C MANE Select NP_036407.1:p.Met11Thr
Search 100 bp 5'
Search 100 bp 3'