Canonical Allele Identifier: CA348287014

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113588126T>A (hg19) ; chr2:g.112830549T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830549T>A , CM000664.2:g.112830549T>A	GRCh38
NC_000002.11:g.113588126T>A , CM000664.1:g.113588126T>A	GRCh37
NC_000002.10:g.113304597T>A	NCBI36
NG_008851.1:g.11231A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.622A>T MANE Select	ENSP00000263341.2:p.Lys208Ter
ENST00000263341.6:c.622A>T	ENSP00000263341.2:p.Lys208Ter
ENST00000491056.5:n.1429A>T
NM_000576.2:c.622A>T	NP_000567.1:p.Lys208Ter
XM_006712496.1:c.388A>T	XP_006712559.1:p.Lys130Ter
XM_017003988.2:c.529A>T	XP_016859477.1:p.Lys177Ter
NM_000576.3:c.622A>T MANE Select	NP_000567.1:p.Lys208Ter