Canonical Allele Identifier: CA1279938262

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830720_112830721delinsCT , CM000664.2:g.112830720_112830721delinsCT	GRCh38
NC_000002.11:g.113588297_113588298delinsCT , CM000664.1:g.113588297_113588298delinsCT	GRCh37
NC_000002.10:g.113304768_113304769delinsCT	NCBI36
NG_008851.1:g.11059_11060delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-148_598-147delinsAG MANE Select	ENSP00000263341.2:n.598-148_598-147delinsAG
ENST00000263341.6:c.598-148_598-147delinsAG	ENSP00000263341.2:n.598-148_598-147delinsAG
ENST00000491056.5:n.1405-148_1405-147delinsAG
NM_000576.2:c.598-148_598-147delinsAG	NP_000567.1:n.598-148_598-147delinsAG
XM_006712496.1:c.364-148_364-147delinsAG	XP_006712559.1:n.364-148_364-147delinsAG
XM_017003988.2:c.505-148_505-147delinsAG	XP_016859477.1:n.505-148_505-147delinsAG
NM_000576.3:c.598-148_598-147delinsAG MANE Select	NP_000567.1:n.598-148_598-147delinsAG