Canonical Allele Identifier: CA1279938188

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830546_112830553delinsTCTTTGGG , CM000664.2:g.112830546_112830553delinsTCTTTGGG	GRCh38
NC_000002.11:g.113588123_113588130delinsTCTTTGGG , CM000664.1:g.113588123_113588130delinsTCTTTGGG	GRCh37
NC_000002.10:g.113304594_113304601delinsTCTTTGGG	NCBI36
NG_008851.1:g.11227_11234delinsCCCAAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.618_625delinsCCCAAAGA MANE Select	ENSP00000263341.2:p.Tyr206=
ENST00000263341.6:c.618_625delinsCCCAAAGA	ENSP00000263341.2:p.Tyr206=
ENST00000491056.5:n.1425_1432delinsCCCAAAGA
NM_000576.2:c.618_625delinsCCCAAAGA	NP_000567.1:p.Tyr206=
XM_006712496.1:c.384_391delinsCCCAAAGA	XP_006712559.1:p.Tyr128=
XM_017003988.2:c.525_532delinsCCCAAAGA	XP_016859477.1:p.Tyr175=
NM_000576.3:c.618_625delinsCCCAAAGA MANE Select	NP_000567.1:p.Tyr206=