Canonical Allele Identifier: CA348286911

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113588110T>A (hg19) ; chr2:g.112830533T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830533T>A , CM000664.2:g.112830533T>A	GRCh38
NC_000002.11:g.113588110T>A , CM000664.1:g.113588110T>A	GRCh37
NC_000002.10:g.113304581T>A	NCBI36
NG_008851.1:g.11247A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.638A>T MANE Select	ENSP00000263341.2:p.Lys213Met
ENST00000263341.6:c.638A>T	ENSP00000263341.2:p.Lys213Met
ENST00000491056.5:n.1445A>T
NM_000576.2:c.638A>T	NP_000567.1:p.Lys213Met
XM_006712496.1:c.404A>T	XP_006712559.1:p.Lys135Met
XM_017003988.2:c.545A>T	XP_016859477.1:p.Lys182Met
NM_000576.3:c.638A>T MANE Select	NP_000567.1:p.Lys213Met