Canonical Allele Identifier: CA348288462

Gene: IL1B

Linked Data

• dbSNP Id: rs1380407701
• gnomAD v2: 2-113590400-G-A
• gnomAD v4: 2-112832823-G-A
• MyVariant Identifiers: chr2:g.113590400G>A (hg19) ; chr2:g.112832823G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832823G>A , CM000664.2:g.112832823G>A	GRCh38
NC_000002.11:g.113590400G>A , CM000664.1:g.113590400G>A	GRCh37
NC_000002.10:g.113306871G>A	NCBI36
NG_008851.1:g.8957C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.305C>T MANE Select	ENSP00000263341.2:p.Pro102Leu
ENST00000263341.6:c.305C>T	ENSP00000263341.2:p.Pro102Leu
ENST00000416750.1:c.305C>T	ENSP00000400854.1:p.Pro102Leu
ENST00000418817.5:c.305C>T	ENSP00000407219.1:p.Pro102Leu
ENST00000432018.5:c.305C>T	ENSP00000409680.1:p.Pro102Leu
ENST00000487639.1:n.206C>T
ENST00000491056.5:n.1112C>T
NM_000576.2:c.305C>T	NP_000567.1:p.Pro102Leu
XM_006712496.1:c.71C>T	XP_006712559.1:p.Pro24Leu
XM_017003988.2:c.212C>T	XP_016859477.1:p.Pro71Leu
NM_000576.3:c.305C>T MANE Select	NP_000567.1:p.Pro102Leu