Canonical Allele Identifier: CA755258944
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1385932533
gnomAD v3: 2-113106432-G-T
gnomAD v4: 2-113106432-G-T
MyVariant Identifiers: chr2:g.113864009G>T (hg19) chr2:g.113106432G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113106432G>T , CM000664.2:g.113106432G>T GRCh38
NC_000002.11:g.113864009G>T , CM000664.1:g.113864009G>T GRCh37
NC_000002.10:g.113580480G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409052.6:c.-471-4684G>T ENSP00000387210.1:n.-471-4684G>T
ENST00000463073.6:n.104-4684G>T
ENST00000465812.6:n.276-782G>T
XM_011511121.1:c.-471-4684G>T XP_011509423.1:n.-471-4684G>T
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