Canonical Allele Identifier: CA1280040318
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs1685659028
gnomAD v4: 2-113062321-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062321C>G , CM000664.2:g.113062321C>G GRCh38
NC_000002.11:g.113819898C>G , CM000664.1:g.113819898C>G GRCh37
NC_000002.10:g.113536369C>G NCBI36
NG_031864.1:g.8684C>G , LRG_730:g.8684C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.243+70C>G ENSP00000409262.2:n.243+70C>G
ENST00000393200.7:c.243+70C>G MANE Select ENSP00000376896.2:n.243+70C>G
ENST00000346807.7:c.243+70C>G ENSP00000259212.3:n.243+70C>G
ENST00000393200.6:c.243+70C>G ENSP00000376896.2:n.243+70C>G
ENST00000437409.1:c.243+70C>G ENSP00000409262.1:n.243+70C>G
NM_012275.2:c.243+70C>G , LRG_730t2:c.243+70C>G NP_036407.1:n.243+70C>G
NM_173170.1:c.243+70C>G , LRG_730t1:c.243+70C>G NP_775262.1:n.243+70C>G
NM_012275.3:c.243+70C>G MANE Select NP_036407.1:n.243+70C>G
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