Canonical Allele Identifier: CA11321020
Gene: IL1R1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1120036
ClinVar RCV Id: RCV001543149
dbSNP Id: rs13019803

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102159742C>T , CM000664.2:g.102159742C>T GRCh38
NC_000002.11:g.102776202C>T , CM000664.1:g.102776202C>T GRCh37
NC_000002.10:g.102142634C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000410023.6:c.61+1957C>T MANE Select ENSP00000386380.1:n.61+1957C>T
ENST00000409288.5:c.61+1957C>T ENSP00000386478.1:n.61+1957C>T
ENST00000409329.5:c.61+1957C>T ENSP00000387131.1:n.61+1957C>T
ENST00000409589.5:c.61+1957C>T ENSP00000386555.1:n.61+1957C>T
ENST00000409929.5:c.61+1957C>T ENSP00000386776.1:n.61+1957C>T
ENST00000410023.5:c.61+1957C>T ENSP00000386380.1:n.61+1957C>T
ENST00000413623.5:c.61+1957C>T ENSP00000407017.1:n.61+1957C>T
ENST00000424272.5:c.61+1957C>T ENSP00000415366.1:n.61+1957C>T
ENST00000428279.5:c.-371-5032C>T ENSP00000410461.1:n.-371-5032C>T
ENST00000430171.1:c.61+1957C>T ENSP00000408101.1:n.61+1957C>T
ENST00000442590.5:c.61+1957C>T ENSP00000393296.1:n.61+1957C>T
ENST00000450319.5:c.61+1957C>T ENSP00000411627.1:n.61+1957C>T
ENST00000452403.5:c.61+1957C>T ENSP00000401646.1:n.61+1957C>T
NM_000877.3:c.61+1957C>T NP_000868.1:n.61+1957C>T
NM_001288706.1:c.61+1957C>T NP_001275635.1:n.61+1957C>T
XM_005263929.1:c.61+1957C>T XP_005263986.1:n.61+1957C>T
XM_005263930.3:c.61+1957C>T XP_005263987.1:n.61+1957C>T
XM_005263931.1:c.61+1957C>T XP_005263988.1:n.61+1957C>T
XM_005263932.1:c.61+1957C>T XP_005263989.1:n.61+1957C>T
XM_005263933.3:c.61+1957C>T XP_005263990.1:n.61+1957C>T
XM_005263934.3:c.61+1957C>T XP_005263991.1:n.61+1957C>T
XM_011511114.1:c.61+1957C>T XP_011509416.1:n.61+1957C>T
XM_011511115.1:c.61+1957C>T XP_011509417.1:n.61+1957C>T
XM_011511116.1:c.61+1957C>T XP_011509418.1:n.61+1957C>T
XM_011511117.1:c.61+1957C>T XP_011509419.1:n.61+1957C>T
XM_011511118.1:c.61+1957C>T XP_011509420.1:n.61+1957C>T
XM_011511119.1:c.-476+1957C>T XP_011509421.1:n.-476+1957C>T
XM_011511120.1:c.61+1957C>T XP_011509422.1:n.61+1957C>T
NM_001320978.1:c.61+1957C>T NP_001307907.1:n.61+1957C>T
NM_001320980.1:c.61+1957C>T NP_001307909.1:n.61+1957C>T
NM_001320981.1:c.61+1957C>T NP_001307910.1:n.61+1957C>T
NM_001320982.1:c.61+1957C>T NP_001307911.1:n.61+1957C>T
NM_001320983.1:c.-371-5032C>T NP_001307912.1:n.-371-5032C>T
NM_001320984.1:c.-299+1957C>T NP_001307913.1:n.-299+1957C>T
NM_001320985.1:c.-476+1957C>T NP_001307914.1:n.-476+1957C>T
NM_001320986.1:c.61+1957C>T NP_001307915.1:n.61+1957C>T
XM_005263930.4:c.61+1957C>T XP_005263987.1:n.61+1957C>T
XM_005263934.4:c.61+1957C>T XP_005263991.1:n.61+1957C>T
XM_011511115.2:c.61+1957C>T XP_011509417.1:n.61+1957C>T
XM_011511118.2:c.61+1957C>T XP_011509420.1:n.61+1957C>T
XM_017003989.1:c.61+1957C>T XP_016859478.1:n.61+1957C>T
NM_000877.4:c.61+1957C>T MANE Select NP_000868.1:n.61+1957C>T
NM_001288706.2:c.61+1957C>T NP_001275635.1:n.61+1957C>T
NM_001320978.2:c.61+1957C>T NP_001307907.1:n.61+1957C>T
NM_001320980.2:c.61+1957C>T NP_001307909.1:n.61+1957C>T
NM_001320981.2:c.61+1957C>T NP_001307910.1:n.61+1957C>T
NM_001320982.2:c.61+1957C>T NP_001307911.1:n.61+1957C>T
NM_001320986.2:c.61+1957C>T NP_001307915.1:n.61+1957C>T