Canonical Allele Identifier: CA1837321

Gene: IL1B

Linked Data

• dbSNP Id: rs767816421
• ExAC: 2:113590399 A / C
• gnomAD v2: 2-113590399-A-C
• gnomAD v3: 2-112832822-A-C
• gnomAD v4: 2-112832822-A-C
• MyVariant Identifiers: chr2:g.113590399A>C (hg19) ; chr2:g.112832822A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832822A>C , CM000664.2:g.112832822A>C	GRCh38
NC_000002.11:g.113590399A>C , CM000664.1:g.113590399A>C	GRCh37
NC_000002.10:g.113306870A>C	NCBI36
NG_008851.1:g.8958T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.306T>G MANE Select	ENSP00000263341.2:p.Pro102=
ENST00000263341.6:c.306T>G	ENSP00000263341.2:p.Pro102=
ENST00000416750.1:c.306T>G	ENSP00000400854.1:p.Pro102=
ENST00000418817.5:c.306T>G	ENSP00000407219.1:p.Pro102=
ENST00000432018.5:c.306T>G	ENSP00000409680.1:p.Pro102=
ENST00000487639.1:n.207T>G
ENST00000491056.5:n.1113T>G
NM_000576.2:c.306T>G	NP_000567.1:p.Pro102=
XM_006712496.1:c.72T>G	XP_006712559.1:p.Pro24=
XM_017003988.2:c.213T>G	XP_016859477.1:p.Pro71=
NM_000576.3:c.306T>G MANE Select	NP_000567.1:p.Pro102=