Canonical Allele Identifier: CA348287060
Gene: IL1B HGNC NCBI

Linked Data

gnomAD v4: 2-112830560-T-C
MyVariant Identifiers: chr2:g.113588137T>C (hg19) chr2:g.112830560T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830560T>C , CM000664.2:g.112830560T>C GRCh38
NC_000002.11:g.113588137T>C , CM000664.1:g.113588137T>C GRCh37
NC_000002.10:g.113304608T>C NCBI36
NG_008851.1:g.11220A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.611A>G MANE Select ENSP00000263341.2:p.Lys204Arg
ENST00000263341.6:c.611A>G ENSP00000263341.2:p.Lys204Arg
ENST00000491056.5:n.1418A>G
NM_000576.2:c.611A>G NP_000567.1:p.Lys204Arg
XM_006712496.1:c.377A>G XP_006712559.1:p.Lys126Arg
XM_017003988.2:c.518A>G XP_016859477.1:p.Lys173Arg
NM_000576.3:c.611A>G MANE Select NP_000567.1:p.Lys204Arg
Search 100 bp 5'
Search 100 bp 3'