Canonical Allele Identifier: CA2700199879
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs2104432693
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113117794A>T , CM000664.2:g.113117794A>T GRCh38
NC_000002.11:g.113875371A>T , CM000664.1:g.113875371A>T GRCh37
NC_000002.10:g.113591842A>T NCBI36
NG_021240.1:g.4902A>T , LRG_188:g.4902A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-272-2272A>T ENSP00000387210.1:n.-272-2272A>T
ENST00000465812.6:n.775+129A>T
ENST00000409052.5:c.-272-2272A>T ENSP00000387210.1:n.-272-2272A>T
XM_011511121.1:c.-272-2272A>T XP_011509423.1:n.-272-2272A>T
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