Canonical Allele Identifier: CA754302783

Gene: IL1R1

Linked Data

• dbSNP Id: rs2234650
• gnomAD v4: 2-102141867-C-G
• MyVariant Identifiers: chr2:g.102758327C>G (hg19) ; chr2:g.102141867C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102141867C>G , CM000664.2:g.102141867C>G	GRCh38
NC_000002.11:g.102758327C>G , CM000664.1:g.102758327C>G	GRCh37
NC_000002.10:g.102124759C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409329.5:c.-83-12074C>G	ENSP00000387131.1:n.-83-12074C>G
ENST00000409589.5:c.-83-12074C>G	ENSP00000386555.1:n.-83-12074C>G
ENST00000409929.5:c.-83-12074C>G	ENSP00000386776.1:n.-83-12074C>G
ENST00000424272.5:c.-83-12074C>G	ENSP00000415366.1:n.-83-12074C>G
ENST00000428279.5:c.-581C>G	ENSP00000410461.1:n.-581C>G
ENST00000450319.5:c.-135C>G	ENSP00000411627.1:n.-135C>G
ENST00000452403.5:c.-83-12074C>G	ENSP00000401646.1:n.-83-12074C>G
NM_001288706.1:c.-83-12074C>G	NP_001275635.1:n.-83-12074C>G
XM_005263929.1:c.-83-12074C>G	XP_005263986.1:n.-83-12074C>G
XM_005263931.1:c.-135C>G	XP_005263988.1:n.-135C>G
XM_005263932.1:c.-83-12074C>G	XP_005263989.1:n.-83-12074C>G
XM_011511115.1:c.-83-12074C>G	XP_011509417.1:n.-83-12074C>G
XM_011511116.1:c.-84+235C>G	XP_011509418.1:n.-84+235C>G
XM_011511117.1:c.-83-12074C>G	XP_011509419.1:n.-83-12074C>G
NM_001320978.1:c.-83-12074C>G	NP_001307907.1:n.-83-12074C>G
NM_001320980.1:c.-83-12074C>G	NP_001307909.1:n.-83-12074C>G
NM_001320981.1:c.-135C>G	NP_001307910.1:n.-135C>G
NM_001320986.1:c.-83-12074C>G	NP_001307915.1:n.-83-12074C>G
XM_011511115.2:c.-83-12074C>G	XP_011509417.1:n.-83-12074C>G
XM_017003989.1:c.-216C>G	XP_016859478.1:n.-216C>G
NM_001288706.2:c.-83-12074C>G	NP_001275635.1:n.-83-12074C>G
NM_001320978.2:c.-83-12074C>G	NP_001307907.1:n.-83-12074C>G
NM_001320980.2:c.-83-12074C>G	NP_001307909.1:n.-83-12074C>G
NM_001320981.2:c.-135C>G	NP_001307910.1:n.-135C>G
NM_001320986.2:c.-83-12074C>G	NP_001307915.1:n.-83-12074C>G