Canonical Allele Identifier: CA348288457

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113590397A>T (hg19) ; chr2:g.112832820A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832820A>T , CM000664.2:g.112832820A>T	GRCh38
NC_000002.11:g.113590397A>T , CM000664.1:g.113590397A>T	GRCh37
NC_000002.10:g.113306868A>T	NCBI36
NG_008851.1:g.8960T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.308T>A MANE Select	ENSP00000263341.2:p.Ile103Asn
ENST00000263341.6:c.308T>A	ENSP00000263341.2:p.Ile103Asn
ENST00000416750.1:c.308T>A	ENSP00000400854.1:p.Ile103Asn
ENST00000418817.5:c.308T>A	ENSP00000407219.1:p.Ile103Asn
ENST00000432018.5:c.308T>A	ENSP00000409680.1:p.Ile103Asn
ENST00000487639.1:n.209T>A
ENST00000491056.5:n.1115T>A
NM_000576.2:c.308T>A	NP_000567.1:p.Ile103Asn
XM_006712496.1:c.74T>A	XP_006712559.1:p.Ile25Asn
XM_017003988.2:c.215T>A	XP_016859477.1:p.Ile72Asn
NM_000576.3:c.308T>A MANE Select	NP_000567.1:p.Ile103Asn