Canonical Allele Identifier: CA53696719
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs901645244
gnomAD v4: 2-112831117-G-T
MyVariant Identifiers: chr2:g.113588694G>T (hg19) chr2:g.112831117G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112831117G>T , CM000664.2:g.112831117G>T GRCh38
NC_000002.11:g.113588694G>T , CM000664.1:g.113588694G>T GRCh37
NC_000002.10:g.113305165G>T NCBI36
NG_008851.1:g.10663C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.597+175C>A MANE Select ENSP00000263341.2:n.597+175C>A
ENST00000263341.6:c.597+175C>A ENSP00000263341.2:n.597+175C>A
ENST00000491056.5:n.1404+175C>A
NM_000576.2:c.597+175C>A NP_000567.1:n.597+175C>A
XM_006712496.1:c.363+175C>A XP_006712559.1:n.363+175C>A
XM_017003988.2:c.504+175C>A XP_016859477.1:n.504+175C>A
NM_000576.3:c.597+175C>A MANE Select NP_000567.1:n.597+175C>A
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