Canonical Allele Identifier: CA1279938429

Gene: IL1B

Linked Data

• dbSNP Id: rs1681979692
• gnomAD v4: 2-112831119-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112831119T>C , CM000664.2:g.112831119T>C	GRCh38
NC_000002.11:g.113588696T>C , CM000664.1:g.113588696T>C	GRCh37
NC_000002.10:g.113305167T>C	NCBI36
NG_008851.1:g.10661A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.597+173A>G MANE Select	ENSP00000263341.2:n.597+173A>G
ENST00000263341.6:c.597+173A>G	ENSP00000263341.2:n.597+173A>G
ENST00000491056.5:n.1404+173A>G
NM_000576.2:c.597+173A>G	NP_000567.1:n.597+173A>G
XM_006712496.1:c.363+173A>G	XP_006712559.1:n.363+173A>G
XM_017003988.2:c.504+173A>G	XP_016859477.1:n.504+173A>G
NM_000576.3:c.597+173A>G MANE Select	NP_000567.1:n.597+173A>G