Canonical Allele Identifier: CA2660746863

Gene: IL1B

Linked Data

• gnomAD v4: 2-112830712-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830712G>C , CM000664.2:g.112830712G>C	GRCh38
NC_000002.11:g.113588289G>C , CM000664.1:g.113588289G>C	GRCh37
NC_000002.10:g.113304760G>C	NCBI36
NG_008851.1:g.11068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-139C>G MANE Select	ENSP00000263341.2:n.598-139C>G
ENST00000263341.6:c.598-139C>G	ENSP00000263341.2:n.598-139C>G
ENST00000491056.5:n.1405-139C>G
NM_000576.2:c.598-139C>G	NP_000567.1:n.598-139C>G
XM_006712496.1:c.364-139C>G	XP_006712559.1:n.364-139C>G
XM_017003988.2:c.505-139C>G	XP_016859477.1:n.505-139C>G
NM_000576.3:c.598-139C>G MANE Select	NP_000567.1:n.598-139C>G