Canonical Allele Identifier: CA754260935

Gene: IL1R2

Linked Data

• dbSNP Id: rs1402625028
• gnomAD v3: 2-101994272-T-C
• gnomAD v4: 2-101994272-T-C
• MyVariant Identifiers: chr2:g.102610734T>C (hg19) ; chr2:g.101994272T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101994272T>C , CM000664.2:g.101994272T>C	GRCh38
NC_000002.11:g.102610734T>C , CM000664.1:g.102610734T>C	GRCh37
NC_000002.10:g.101977166T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000332549.8:c.-62+2261T>C MANE Select	ENSP00000330959.3:n.-62+2261T>C
ENST00000332549.7:c.-62+2261T>C	ENSP00000330959.3:n.-62+2261T>C
ENST00000464994.5:n.74+2239T>C
ENST00000493749.1:n.52+2261T>C
NM_001261419.1:c.-62+2261T>C	NP_001248348.1:n.-62+2261T>C
NM_004633.3:c.-62+2261T>C	NP_004624.1:n.-62+2261T>C
XM_006712734.2:c.-62+2276T>C	XP_006712797.1:n.-62+2276T>C
XM_006712736.2:c.14+2239T>C	XP_006712799.1:n.14+2239T>C
XM_006712734.3:c.-62+2276T>C	XP_006712797.1:n.-62+2276T>C
XM_006712736.3:c.14+2239T>C	XP_006712799.1:n.14+2239T>C
XM_017004889.1:c.-189+2261T>C	XP_016860378.1:n.-189+2261T>C
XM_024453129.1:c.-157+2276T>C	XP_024308897.1:n.-157+2276T>C
NM_004633.4:c.-62+2261T>C MANE Select	NP_004624.1:n.-62+2261T>C
NM_001261419.2:c.-62+2261T>C	NP_001248348.1:n.-62+2261T>C