Canonical Allele Identifier: CA1035145889
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1686628079

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113117736T>C , CM000664.2:g.113117736T>C GRCh38
NC_000002.11:g.113875313T>C , CM000664.1:g.113875313T>C GRCh37
NC_000002.10:g.113591784T>C NCBI36
NG_021240.1:g.4844T>C , LRG_188:g.4844T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-272-2330T>C ENSP00000387210.1:n.-272-2330T>C
ENST00000465812.6:n.775+71T>C
ENST00000409052.5:c.-272-2330T>C ENSP00000387210.1:n.-272-2330T>C
XM_011511121.1:c.-272-2330T>C XP_011509423.1:n.-272-2330T>C