Canonical Allele Identifier: CA755282923
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1316021706
MyVariant Identifiers: chr2:g.113588703T>G (hg19) chr2:g.112831126T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831126T>G , CM000664.2:g.112831126T>G GRCh38
NC_000002.11:g.113588703T>G , CM000664.1:g.113588703T>G GRCh37
NC_000002.10:g.113305174T>G NCBI36
NG_008851.1:g.10654A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.597+166A>C MANE Select ENSP00000263341.2:n.597+166A>C
ENST00000263341.6:c.597+166A>C ENSP00000263341.2:n.597+166A>C
ENST00000491056.5:n.1404+166A>C
NM_000576.2:c.597+166A>C NP_000567.1:n.597+166A>C
XM_006712496.1:c.363+166A>C XP_006712559.1:n.363+166A>C
XM_017003988.2:c.504+166A>C XP_016859477.1:n.504+166A>C
NM_000576.3:c.597+166A>C MANE Select NP_000567.1:n.597+166A>C
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