Canonical Allele Identifier: CA348287059
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1477951328
gnomAD v2: 2-113588137-T-A
gnomAD v3: 2-112830560-T-A
gnomAD v4: 2-112830560-T-A
MyVariant Identifiers: chr2:g.113588137T>A (hg19) chr2:g.112830560T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.611A>T MANE Select ENSP00000263341.2:p.Lys204Ile
ENST00000263341.6:c.611A>T ENSP00000263341.2:p.Lys204Ile
ENST00000491056.5:n.1418A>T
NM_000576.2:c.611A>T NP_000567.1:p.Lys204Ile
XM_006712496.1:c.377A>T XP_006712559.1:p.Lys126Ile
XM_017003988.2:c.518A>T XP_016859477.1:p.Lys173Ile
NM_000576.3:c.611A>T MANE Select NP_000567.1:p.Lys204Ile
Search 100 bp 5'
Search 100 bp 3'