Canonical Allele Identifier: CA755236221
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs1334717180
MyVariant Identifiers: chr2:g.113819908G>A (hg19) chr2:g.113062331G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062331G>A , CM000664.2:g.113062331G>A GRCh38
NC_000002.11:g.113819908G>A , CM000664.1:g.113819908G>A GRCh37
NC_000002.10:g.113536379G>A NCBI36
NG_031864.1:g.8694G>A , LRG_730:g.8694G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.243+80G>A ENSP00000409262.2:n.243+80G>A
ENST00000393200.7:c.243+80G>A MANE Select ENSP00000376896.2:n.243+80G>A
ENST00000346807.7:c.243+80G>A ENSP00000259212.3:n.243+80G>A
ENST00000393200.6:c.243+80G>A ENSP00000376896.2:n.243+80G>A
ENST00000437409.1:c.243+80G>A ENSP00000409262.1:n.243+80G>A
NM_012275.2:c.243+80G>A , LRG_730t2:c.243+80G>A NP_036407.1:n.243+80G>A
NM_173170.1:c.243+80G>A , LRG_730t1:c.243+80G>A NP_775262.1:n.243+80G>A
NM_012275.3:c.243+80G>A MANE Select NP_036407.1:n.243+80G>A
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