Canonical Allele Identifier: CA348286960
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs138009692
gnomAD v3: 2-112830541-C-A
gnomAD v4: 2-112830541-C-A
MyVariant Identifiers: chr2:g.113588118C>A (hg19) chr2:g.112830541C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830541C>A , CM000664.2:g.112830541C>A GRCh38
NC_000002.11:g.113588118C>A , CM000664.1:g.113588118C>A GRCh37
NC_000002.10:g.113304589C>A NCBI36
NG_008851.1:g.11239G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.630G>T MANE Select ENSP00000263341.2:p.Lys210Asn
ENST00000263341.6:c.630G>T ENSP00000263341.2:p.Lys210Asn
ENST00000491056.5:n.1437G>T
NM_000576.2:c.630G>T NP_000567.1:p.Lys210Asn
XM_006712496.1:c.396G>T XP_006712559.1:p.Lys132Asn
XM_017003988.2:c.537G>T XP_016859477.1:p.Lys179Asn
NM_000576.3:c.630G>T MANE Select NP_000567.1:p.Lys210Asn
Search 100 bp 5'
Search 100 bp 3'