Canonical Allele Identifier: CA2536190193

Gene: IL1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830812_112830813dup , CM000664.2:g.112830812_112830813dup	GRCh38
NC_000002.11:g.113588389_113588390dup , CM000664.1:g.113588389_113588390dup	GRCh37
NC_000002.10:g.113304860_113304861dup	NCBI36
NG_008851.1:g.10977_10978dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.598-230_598-229dup MANE Select	ENSP00000263341.2:n.598-230_598-229dup
ENST00000263341.6:c.598-230_598-229dup	ENSP00000263341.2:n.598-230_598-229dup
ENST00000491056.5:n.1405-230_1405-229dup
NM_000576.2:c.598-230_598-229dup	NP_000567.1:n.598-230_598-229dup
XM_006712496.1:c.364-230_364-229dup	XP_006712559.1:n.364-230_364-229dup
XM_017003988.2:c.505-230_505-229dup	XP_016859477.1:n.505-230_505-229dup
NM_000576.3:c.598-230_598-229dup MANE Select	NP_000567.1:n.598-230_598-229dup