Canonical Allele Identifier: CA755284024
Gene: IL1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832890C>G , CM000664.2:g.112832890C>G GRCh38
NC_000002.11:g.113590467C>G , CM000664.1:g.113590467C>G GRCh37
NC_000002.10:g.113306938C>G NCBI36
NG_008851.1:g.8890G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.302-64G>C MANE Select ENSP00000263341.2:n.302-64G>C
ENST00000263341.6:c.302-64G>C ENSP00000263341.2:n.302-64G>C
ENST00000416750.1:c.302-64G>C ENSP00000400854.1:n.302-64G>C
ENST00000418817.5:c.302-64G>C ENSP00000407219.1:n.302-64G>C
ENST00000432018.5:c.302-64G>C ENSP00000409680.1:n.302-64G>C
ENST00000487639.1:n.203-64G>C
ENST00000491056.5:n.1109-64G>C
NM_000576.2:c.302-64G>C NP_000567.1:n.302-64G>C
XM_006712496.1:c.68-64G>C XP_006712559.1:n.68-64G>C
XM_017003988.2:c.209-64G>C XP_016859477.1:n.209-64G>C
NM_000576.3:c.302-64G>C MANE Select NP_000567.1:n.302-64G>C