Canonical Allele Identifier: CA428298881

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113588130G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.618C>T MANE Select	ENSP00000263341.2:p.Tyr206=
ENST00000263341.6:c.618C>T	ENSP00000263341.2:p.Tyr206=
ENST00000491056.5:n.1425C>T
NM_000576.2:c.618C>T	NP_000567.1:p.Tyr206=
XM_006712496.1:c.384C>T	XP_006712559.1:p.Tyr128=
XM_017003988.2:c.525C>T	XP_016859477.1:p.Tyr175=
NM_000576.3:c.618C>T MANE Select	NP_000567.1:p.Tyr206=