Canonical Allele Identifier: CA2660746775

Gene: IL1B

Linked Data

• gnomAD v4: 2-112830641-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830641T>C , CM000664.2:g.112830641T>C	GRCh38
NC_000002.11:g.113588218T>C , CM000664.1:g.113588218T>C	GRCh37
NC_000002.10:g.113304689T>C	NCBI36
NG_008851.1:g.11139A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-68A>G MANE Select	ENSP00000263341.2:n.598-68A>G
ENST00000263341.6:c.598-68A>G	ENSP00000263341.2:n.598-68A>G
ENST00000491056.5:n.1405-68A>G
NM_000576.2:c.598-68A>G	NP_000567.1:n.598-68A>G
XM_006712496.1:c.364-68A>G	XP_006712559.1:n.364-68A>G
XM_017003988.2:c.505-68A>G	XP_016859477.1:n.505-68A>G
NM_000576.3:c.598-68A>G MANE Select	NP_000567.1:n.598-68A>G