Canonical Allele Identifier: CA348287045

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113588133A>T (hg19) ; chr2:g.112830556A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112830556A>T , CM000664.2:g.112830556A>T	GRCh38
NC_000002.11:g.113588133A>T , CM000664.1:g.113588133A>T	GRCh37
NC_000002.10:g.113304604A>T	NCBI36
NG_008851.1:g.11224T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263341.7:c.615T>A MANE Select	ENSP00000263341.2:p.Asn205Lys
ENST00000263341.6:c.615T>A	ENSP00000263341.2:p.Asn205Lys
ENST00000491056.5:n.1422T>A
NM_000576.2:c.615T>A	NP_000567.1:p.Asn205Lys
XM_006712496.1:c.381T>A	XP_006712559.1:p.Asn127Lys
XM_017003988.2:c.522T>A	XP_016859477.1:p.Asn174Lys
NM_000576.3:c.615T>A MANE Select	NP_000567.1:p.Asn205Lys