Canonical Allele Identifier: CA2660746788
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112830653-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830653G>C , CM000664.2:g.112830653G>C GRCh38
NC_000002.11:g.113588230G>C , CM000664.1:g.113588230G>C GRCh37
NC_000002.10:g.113304701G>C NCBI36
NG_008851.1:g.11127C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.598-80C>G MANE Select ENSP00000263341.2:n.598-80C>G
ENST00000263341.6:c.598-80C>G ENSP00000263341.2:n.598-80C>G
ENST00000491056.5:n.1405-80C>G
NM_000576.2:c.598-80C>G NP_000567.1:n.598-80C>G
XM_006712496.1:c.364-80C>G XP_006712559.1:n.364-80C>G
XM_017003988.2:c.505-80C>G XP_016859477.1:n.505-80C>G
NM_000576.3:c.598-80C>G MANE Select NP_000567.1:n.598-80C>G
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