Canonical Allele Identifier: CA53696337
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1008203506
MyVariant Identifiers: chr2:g.112830613G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830613G>A , CM000664.2:g.112830613G>A GRCh38
NC_000002.11:g.113588190G>A , CM000664.1:g.113588190G>A GRCh37
NC_000002.10:g.113304661G>A NCBI36
NG_008851.1:g.11167C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-40C>T MANE Select ENSP00000263341.2:n.598-40C>T
ENST00000263341.6:c.598-40C>T ENSP00000263341.2:n.598-40C>T
ENST00000491056.5:n.1405-40C>T
NM_000576.2:c.598-40C>T NP_000567.1:n.598-40C>T
XM_006712496.1:c.364-40C>T XP_006712559.1:n.364-40C>T
XM_017003988.2:c.505-40C>T XP_016859477.1:n.505-40C>T
NM_000576.3:c.598-40C>T MANE Select NP_000567.1:n.598-40C>T
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