Canonical Allele Identifier: CA535595899
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1272398477
gnomAD v2: 2-113588312-T-C
gnomAD v3: 2-112830735-T-C
gnomAD v4: 2-112830735-T-C
MyVariant Identifiers: chr2:g.113588312T>C (hg19) chr2:g.112830735T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830735T>C , CM000664.2:g.112830735T>C GRCh38
NC_000002.11:g.113588312T>C , CM000664.1:g.113588312T>C GRCh37
NC_000002.10:g.113304783T>C NCBI36
NG_008851.1:g.11045A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-162A>G MANE Select ENSP00000263341.2:n.598-162A>G
ENST00000263341.6:c.598-162A>G ENSP00000263341.2:n.598-162A>G
ENST00000491056.5:n.1405-162A>G
NM_000576.2:c.598-162A>G NP_000567.1:n.598-162A>G
XM_006712496.1:c.364-162A>G XP_006712559.1:n.364-162A>G
XM_017003988.2:c.505-162A>G XP_016859477.1:n.505-162A>G
NM_000576.3:c.598-162A>G MANE Select NP_000567.1:n.598-162A>G
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