Canonical Allele Identifier: CA428298887

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113588139G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830562G>A , CM000664.2:g.112830562G>A	GRCh38
NC_000002.11:g.113588139G>A , CM000664.1:g.113588139G>A	GRCh37
NC_000002.10:g.113304610G>A	NCBI36
NG_008851.1:g.11218C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.609C>T MANE Select	ENSP00000263341.2:p.Pro203=
ENST00000263341.6:c.609C>T	ENSP00000263341.2:p.Pro203=
ENST00000491056.5:n.1416C>T
NM_000576.2:c.609C>T	NP_000567.1:p.Pro203=
XM_006712496.1:c.375C>T	XP_006712559.1:p.Pro125=
XM_017003988.2:c.516C>T	XP_016859477.1:p.Pro172=
NM_000576.3:c.609C>T MANE Select	NP_000567.1:p.Pro203=