Canonical Allele Identifier: CA755268638
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs530907401
gnomAD v3: 2-113117729-A-G
gnomAD v4: 2-113117729-A-G
MyVariant Identifiers: chr2:g.113875306A>G (hg19) chr2:g.113117729A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113117729A>G , CM000664.2:g.113117729A>G GRCh38
NC_000002.11:g.113875306A>G , CM000664.1:g.113875306A>G GRCh37
NC_000002.10:g.113591777A>G NCBI36
NG_021240.1:g.4837A>G , LRG_188:g.4837A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-272-2337A>G ENSP00000387210.1:n.-272-2337A>G
ENST00000465812.6:n.775+64A>G
ENST00000409052.5:c.-272-2337A>G ENSP00000387210.1:n.-272-2337A>G
XM_011511121.1:c.-272-2337A>G XP_011509423.1:n.-272-2337A>G
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