Canonical Allele Identifier: CA348287034

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113588130G>T (hg19) ; chr2:g.112830553G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830553G>T , CM000664.2:g.112830553G>T	GRCh38
NC_000002.11:g.113588130G>T , CM000664.1:g.113588130G>T	GRCh37
NC_000002.10:g.113304601G>T	NCBI36
NG_008851.1:g.11227C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.618C>A MANE Select	ENSP00000263341.2:p.Tyr206Ter
ENST00000263341.6:c.618C>A	ENSP00000263341.2:p.Tyr206Ter
ENST00000491056.5:n.1425C>A
NM_000576.2:c.618C>A	NP_000567.1:p.Tyr206Ter
XM_006712496.1:c.384C>A	XP_006712559.1:p.Tyr128Ter
XM_017003988.2:c.525C>A	XP_016859477.1:p.Tyr175Ter
NM_000576.3:c.618C>A MANE Select	NP_000567.1:p.Tyr206Ter