Canonical Allele Identifier: CA348287065
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1169593578
gnomAD v2: 2-113588138-T-C
gnomAD v3: 2-112830561-T-C
gnomAD v4: 2-112830561-T-C
MyVariant Identifiers: chr2:g.113588138T>C (hg19) chr2:g.112830561T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830561T>C , CM000664.2:g.112830561T>C GRCh38
NC_000002.11:g.113588138T>C , CM000664.1:g.113588138T>C GRCh37
NC_000002.10:g.113304609T>C NCBI36
NG_008851.1:g.11219A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.610A>G MANE Select ENSP00000263341.2:p.Lys204Glu
ENST00000263341.6:c.610A>G ENSP00000263341.2:p.Lys204Glu
ENST00000491056.5:n.1417A>G
NM_000576.2:c.610A>G NP_000567.1:p.Lys204Glu
XM_006712496.1:c.376A>G XP_006712559.1:p.Lys126Glu
XM_017003988.2:c.517A>G XP_016859477.1:p.Lys173Glu
NM_000576.3:c.610A>G MANE Select NP_000567.1:p.Lys204Glu
Search 100 bp 5'
Search 100 bp 3'