Canonical Allele Identifier: CA348287076
Gene: IL1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113588141G>T (hg19) chr2:g.112830564G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830564G>T , CM000664.2:g.112830564G>T GRCh38
NC_000002.11:g.113588141G>T , CM000664.1:g.113588141G>T GRCh37
NC_000002.10:g.113304612G>T NCBI36
NG_008851.1:g.11216C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.607C>A MANE Select ENSP00000263341.2:p.Pro203Thr
ENST00000263341.6:c.607C>A ENSP00000263341.2:p.Pro203Thr
ENST00000491056.5:n.1414C>A
NM_000576.2:c.607C>A NP_000567.1:p.Pro203Thr
XM_006712496.1:c.373C>A XP_006712559.1:p.Pro125Thr
XM_017003988.2:c.514C>A XP_016859477.1:p.Pro172Thr
NM_000576.3:c.607C>A MANE Select NP_000567.1:p.Pro203Thr
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Search 100 bp 3'