Canonical Allele Identifier: CA428299775
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113590393G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832816G>A , CM000664.2:g.112832816G>A GRCh38
NC_000002.11:g.113590393G>A , CM000664.1:g.113590393G>A GRCh37
NC_000002.10:g.113306864G>A NCBI36
NG_008851.1:g.8964C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.312C>T MANE Select ENSP00000263341.2:p.Phe104=
ENST00000263341.6:c.312C>T ENSP00000263341.2:p.Phe104=
ENST00000416750.1:c.312C>T ENSP00000400854.1:p.Phe104=
ENST00000418817.5:c.312C>T ENSP00000407219.1:p.Phe104=
ENST00000432018.5:c.312C>T ENSP00000409680.1:p.Phe104=
ENST00000487639.1:n.213C>T
ENST00000491056.5:n.1119C>T
NM_000576.2:c.312C>T NP_000567.1:p.Phe104=
XM_006712496.1:c.78C>T XP_006712559.1:p.Phe26=
XM_017003988.2:c.219C>T XP_016859477.1:p.Phe73=
NM_000576.3:c.312C>T MANE Select NP_000567.1:p.Phe104=