Canonical Allele Identifier: CA1279938441
Gene: IL1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831133C= , CM000664.2:g.112831133C= GRCh38
NC_000002.11:g.113588710C= , CM000664.1:g.113588710C= GRCh37
NC_000002.10:g.113305181C= NCBI36
NG_008851.1:g.10647G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.597+159G= MANE Select ENSP00000263341.2:n.597+159G=
ENST00000263341.6:c.597+159G= ENSP00000263341.2:n.597+159G=
ENST00000491056.5:n.1404+159G=
NM_000576.2:c.597+159G= NP_000567.1:n.597+159G=
XM_006712496.1:c.363+159G= XP_006712559.1:n.363+159G=
XM_017003988.2:c.504+159G= XP_016859477.1:n.504+159G=
NM_000576.3:c.597+159G= MANE Select NP_000567.1:n.597+159G=