Canonical Allele Identifier: CA1838392

Gene: IL36RN

Linked Data

• ClinVar Variation Id: 529885
• ClinVar RCV Id: RCV000635394 ; RCV001200639 ; RCV002263868
• dbSNP Id: rs372880215
• ExAC: 2:113819815 C / T
• gnomAD v2: 2-113819815-C-T
• gnomAD v3: 2-113062238-C-T
• gnomAD v4: 2-113062238-C-T
• MyVariant Identifiers: chr2:g.113819815C>T (hg19) ; chr2:g.113062238C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062238C>T , CM000664.2:g.113062238C>T	GRCh38
NC_000002.11:g.113819815C>T , CM000664.1:g.113819815C>T	GRCh37
NC_000002.10:g.113536286C>T	NCBI36
NG_031864.1:g.8601C>T , LRG_730:g.8601C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000437409.2:c.230C>T	ENSP00000409262.2:p.Thr77Ile
ENST00000393200.7:c.230C>T MANE Select	ENSP00000376896.2:p.Thr77Ile
ENST00000346807.7:c.230C>T	ENSP00000259212.3:p.Thr77Ile
ENST00000393200.6:c.230C>T	ENSP00000376896.2:p.Thr77Ile
ENST00000437409.1:c.230C>T	ENSP00000409262.1:p.Thr77Ile
NM_012275.2:c.230C>T , LRG_730t2:c.230C>T	NP_036407.1:p.Thr77Ile
NM_173170.1:c.230C>T , LRG_730t1:c.230C>T	NP_775262.1:p.Thr77Ile
NM_012275.3:c.230C>T MANE Select	NP_036407.1:p.Thr77Ile