Canonical Allele Identifier: CA2660746783
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112830650-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830650C>T , CM000664.2:g.112830650C>T GRCh38
NC_000002.11:g.113588227C>T , CM000664.1:g.113588227C>T GRCh37
NC_000002.10:g.113304698C>T NCBI36
NG_008851.1:g.11130G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-77G>A MANE Select ENSP00000263341.2:n.598-77G>A
ENST00000263341.6:c.598-77G>A ENSP00000263341.2:n.598-77G>A
ENST00000491056.5:n.1405-77G>A
NM_000576.2:c.598-77G>A NP_000567.1:n.598-77G>A
XM_006712496.1:c.364-77G>A XP_006712559.1:n.364-77G>A
XM_017003988.2:c.505-77G>A XP_016859477.1:n.505-77G>A
NM_000576.3:c.598-77G>A MANE Select NP_000567.1:n.598-77G>A
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