Canonical Allele Identifier: CA348287080

Gene: IL1B

Linked Data

• dbSNP Id: rs1681961659
• gnomAD v4: 2-112830565-A-T
• MyVariant Identifiers: chr2:g.113588142A>T (hg19) ; chr2:g.112830565A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830565A>T , CM000664.2:g.112830565A>T	GRCh38
NC_000002.11:g.113588142A>T , CM000664.1:g.113588142A>T	GRCh37
NC_000002.10:g.113304613A>T	NCBI36
NG_008851.1:g.11215T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.606T>A MANE Select	ENSP00000263341.2:p.Asp202Glu
ENST00000263341.6:c.606T>A	ENSP00000263341.2:p.Asp202Glu
ENST00000491056.5:n.1413T>A
NM_000576.2:c.606T>A	NP_000567.1:p.Asp202Glu
XM_006712496.1:c.372T>A	XP_006712559.1:p.Asp124Glu
XM_017003988.2:c.513T>A	XP_016859477.1:p.Asp171Glu
NM_000576.3:c.606T>A MANE Select	NP_000567.1:p.Asp202Glu