Canonical Allele Identifier: CA1279938285

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830790_112830791delinsTG , CM000664.2:g.112830790_112830791delinsTG	GRCh38
NC_000002.11:g.113588367_113588368delinsTG , CM000664.1:g.113588367_113588368delinsTG	GRCh37
NC_000002.10:g.113304838_113304839delinsTG	NCBI36
NG_008851.1:g.10989_10990delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-218_598-217delinsCA MANE Select	ENSP00000263341.2:n.598-218_598-217delinsCA
ENST00000263341.6:c.598-218_598-217delinsCA	ENSP00000263341.2:n.598-218_598-217delinsCA
ENST00000491056.5:n.1405-218_1405-217delinsCA
NM_000576.2:c.598-218_598-217delinsCA	NP_000567.1:n.598-218_598-217delinsCA
XM_006712496.1:c.364-218_364-217delinsCA	XP_006712559.1:n.364-218_364-217delinsCA
XM_017003988.2:c.505-218_505-217delinsCA	XP_016859477.1:n.505-218_505-217delinsCA
NM_000576.3:c.598-218_598-217delinsCA MANE Select	NP_000567.1:n.598-218_598-217delinsCA