Canonical Allele Identifier: CA535231702
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1353357763
gnomAD v2: 2-113863853-CAAAGGGATAGTGAAT-C
gnomAD v3: 2-113106276-CAAAGGGATAGTGAAT-C
gnomAD v4: 2-113106276-CAAAGGGATAGTGAAT-C
MyVariant Identifiers: chr2:g.113863854_113863868del (hg19) chr2:g.113106277_113106291del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113106281_113106295del , CM000664.2:g.113106281_113106295del GRCh38
NC_000002.11:g.113863858_113863872del , CM000664.1:g.113863858_113863872del GRCh37
NC_000002.10:g.113580329_113580343del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-471-4835_-471-4821del ENSP00000387210.1:n.-471-4835_-471-4821del
ENST00000463073.6:n.104-4835_104-4821del
ENST00000465812.6:n.276-933_276-919del
XM_011511121.1:c.-471-4835_-471-4821del XP_011509423.1:n.-471-4835_-471-4821del
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