Canonical Allele Identifier: CA2577073781

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830604G>T , CM000664.2:g.112830604G>T	GRCh38
NC_000002.11:g.113588181G>T , CM000664.1:g.113588181G>T	GRCh37
NC_000002.10:g.113304652G>T	NCBI36
NG_008851.1:g.11176C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-31C>A MANE Select	ENSP00000263341.2:n.598-31C>A
ENST00000263341.6:c.598-31C>A	ENSP00000263341.2:n.598-31C>A
ENST00000491056.5:n.1405-31C>A
NM_000576.2:c.598-31C>A	NP_000567.1:n.598-31C>A
XM_006712496.1:c.364-31C>A	XP_006712559.1:n.364-31C>A
XM_017003988.2:c.505-31C>A	XP_016859477.1:n.505-31C>A
NM_000576.3:c.598-31C>A MANE Select	NP_000567.1:n.598-31C>A