Canonical Allele Identifier: CA348290171

Gene: IL36RN

Linked Data

• gnomAD v4: 2-113062243-A-G
• MyVariant Identifiers: chr2:g.113819820A>G (hg19) ; chr2:g.113062243A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062243A>G , CM000664.2:g.113062243A>G	GRCh38
NC_000002.11:g.113819820A>G , CM000664.1:g.113819820A>G	GRCh37
NC_000002.10:g.113536291A>G	NCBI36
NG_031864.1:g.8606A>G , LRG_730:g.8606A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.235A>G	ENSP00000409262.2:p.Thr79Ala
ENST00000393200.7:c.235A>G MANE Select	ENSP00000376896.2:p.Thr79Ala
ENST00000346807.7:c.235A>G	ENSP00000259212.3:p.Thr79Ala
ENST00000393200.6:c.235A>G	ENSP00000376896.2:p.Thr79Ala
ENST00000437409.1:c.235A>G	ENSP00000409262.1:p.Thr79Ala
NM_012275.2:c.235A>G , LRG_730t2:c.235A>G	NP_036407.1:p.Thr79Ala
NM_173170.1:c.235A>G , LRG_730t1:c.235A>G	NP_775262.1:p.Thr79Ala
NM_012275.3:c.235A>G MANE Select	NP_036407.1:p.Thr79Ala