Canonical Allele Identifier: CA2660747027
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112831146-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831146T>C , CM000664.2:g.112831146T>C GRCh38
NC_000002.11:g.113588723T>C , CM000664.1:g.113588723T>C GRCh37
NC_000002.10:g.113305194T>C NCBI36
NG_008851.1:g.10634A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.597+146A>G MANE Select ENSP00000263341.2:n.597+146A>G
ENST00000263341.6:c.597+146A>G ENSP00000263341.2:n.597+146A>G
ENST00000487639.1:n.644A>G
ENST00000491056.5:n.1404+146A>G
NM_000576.2:c.597+146A>G NP_000567.1:n.597+146A>G
XM_006712496.1:c.363+146A>G XP_006712559.1:n.363+146A>G
XM_017003988.2:c.504+146A>G XP_016859477.1:n.504+146A>G
NM_000576.3:c.597+146A>G MANE Select NP_000567.1:n.597+146A>G
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