Canonical Allele Identifier: CA535231705
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1461806769
gnomAD v2: 2-113863873-A-G
gnomAD v3: 2-113106296-A-G
gnomAD v4: 2-113106296-A-G
MyVariant Identifiers: chr2:g.113863873A>G (hg19) chr2:g.113106296A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113106296A>G , CM000664.2:g.113106296A>G GRCh38
NC_000002.11:g.113863873A>G , CM000664.1:g.113863873A>G GRCh37
NC_000002.10:g.113580344A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409052.6:c.-471-4820A>G ENSP00000387210.1:n.-471-4820A>G
ENST00000463073.6:n.104-4820A>G
ENST00000465812.6:n.276-918A>G
XM_011511121.1:c.-471-4820A>G XP_011509423.1:n.-471-4820A>G
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