Canonical Allele Identifier: CA2660764559

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113121745-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113121745T>C , CM000664.2:g.113121745T>C	GRCh38
NC_000002.11:g.113879322T>C , CM000664.1:g.113879322T>C	GRCh37
NC_000002.10:g.113595793T>C	NCBI36
NG_021240.1:g.8853T>C , LRG_188:g.8853T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-39+127T>C	ENSP00000387210.1:n.-39+127T>C
ENST00000696881.1:c.-39+127T>C	ENSP00000512949.1:n.-39+127T>C
ENST00000259206.9:c.73+1617T>C	ENSP00000259206.5:n.73+1617T>C
ENST00000354115.6:c.10+3717T>C	ENSP00000329072.3:n.10+3717T>C
ENST00000361779.7:c.-39+127T>C	ENSP00000354816.3:n.-39+127T>C
ENST00000409052.5:c.-39+127T>C	ENSP00000387210.1:n.-39+127T>C
ENST00000486167.1:n.48+3717T>C
NM_000577.4:c.10+3717T>C	NP_000568.1:n.10+3717T>C
NM_173841.2:c.73+1617T>C , LRG_188t1:c.73+1617T>C	NP_776213.1:n.73+1617T>C
NM_173843.2:c.-39+127T>C	NP_776215.1:n.-39+127T>C
XM_006712497.2:c.-39+127T>C	XP_006712560.1:n.-39+127T>C
XM_011511121.1:c.-39+127T>C	XP_011509423.1:n.-39+127T>C
NM_001318914.1:c.-39+127T>C	NP_001305843.1:n.-39+127T>C
NM_000577.5:c.10+3717T>C	NP_000568.1:n.10+3717T>C
NM_001318914.2:c.-39+127T>C	NP_001305843.1:n.-39+127T>C
NM_173843.3:c.-39+127T>C	NP_776215.1:n.-39+127T>C
NM_173841.3:c.73+1617T>C	NP_776213.1:n.73+1617T>C