Canonical Allele Identifier: CA1279938298

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830813_112830814delinsTG , CM000664.2:g.112830813_112830814delinsTG	GRCh38
NC_000002.11:g.113588390_113588391delinsTG , CM000664.1:g.113588390_113588391delinsTG	GRCh37
NC_000002.10:g.113304861_113304862delinsTG	NCBI36
NG_008851.1:g.10966_10967delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-241_598-240delinsCA MANE Select	ENSP00000263341.2:n.598-241_598-240delinsCA
ENST00000263341.6:c.598-241_598-240delinsCA	ENSP00000263341.2:n.598-241_598-240delinsCA
ENST00000491056.5:n.1405-241_1405-240delinsCA
NM_000576.2:c.598-241_598-240delinsCA	NP_000567.1:n.598-241_598-240delinsCA
XM_006712496.1:c.364-241_364-240delinsCA	XP_006712559.1:n.364-241_364-240delinsCA
XM_017003988.2:c.505-241_505-240delinsCA	XP_016859477.1:n.505-241_505-240delinsCA
NM_000576.3:c.598-241_598-240delinsCA MANE Select	NP_000567.1:n.598-241_598-240delinsCA