Canonical Allele Identifier: CA428298876
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113588127T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830550T>C , CM000664.2:g.112830550T>C GRCh38
NC_000002.11:g.113588127T>C , CM000664.1:g.113588127T>C GRCh37
NC_000002.10:g.113304598T>C NCBI36
NG_008851.1:g.11230A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.621A>G MANE Select ENSP00000263341.2:p.Pro207=
ENST00000263341.6:c.621A>G ENSP00000263341.2:p.Pro207=
ENST00000491056.5:n.1428A>G
NM_000576.2:c.621A>G NP_000567.1:p.Pro207=
XM_006712496.1:c.387A>G XP_006712559.1:p.Pro129=
XM_017003988.2:c.528A>G XP_016859477.1:p.Pro176=
NM_000576.3:c.621A>G MANE Select NP_000567.1:p.Pro207=
Search 100 bp 5'
Search 100 bp 3'