Canonical Allele Identifier: CA1035140799
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1686387359
gnomAD v3: 2-113106299-C-G
gnomAD v4: 2-113106299-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113106299C>G , CM000664.2:g.113106299C>G GRCh38
NC_000002.11:g.113863876C>G , CM000664.1:g.113863876C>G GRCh37
NC_000002.10:g.113580347C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409052.6:c.-471-4817C>G ENSP00000387210.1:n.-471-4817C>G
ENST00000463073.6:n.104-4817C>G
ENST00000465812.6:n.276-915C>G
XM_011511121.1:c.-471-4817C>G XP_011509423.1:n.-471-4817C>G
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