Canonical Allele Identifier: CA535235059
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1357426278
gnomAD v2: 2-113875373-C-T
gnomAD v3: 2-113117796-C-T
gnomAD v4: 2-113117796-C-T
MyVariant Identifiers: chr2:g.113875373C>T (hg19) chr2:g.113117796C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113117796C>T , CM000664.2:g.113117796C>T GRCh38
NC_000002.11:g.113875373C>T , CM000664.1:g.113875373C>T GRCh37
NC_000002.10:g.113591844C>T NCBI36
NG_021240.1:g.4904C>T , LRG_188:g.4904C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-272-2270C>T ENSP00000387210.1:n.-272-2270C>T
ENST00000465812.6:n.775+131C>T
ENST00000409052.5:c.-272-2270C>T ENSP00000387210.1:n.-272-2270C>T
XM_011511121.1:c.-272-2270C>T XP_011509423.1:n.-272-2270C>T
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