Canonical Allele Identifier: CA53696421
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs75143301
MyVariant Identifiers: chr2:g.113588340C>A (hg19) chr2:g.112830763C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830763C>A , CM000664.2:g.112830763C>A GRCh38
NC_000002.11:g.113588340C>A , CM000664.1:g.113588340C>A GRCh37
NC_000002.10:g.113304811C>A NCBI36
NG_008851.1:g.11017G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.598-190G>T MANE Select ENSP00000263341.2:n.598-190G>T
ENST00000263341.6:c.598-190G>T ENSP00000263341.2:n.598-190G>T
ENST00000491056.5:n.1405-190G>T
NM_000576.2:c.598-190G>T NP_000567.1:n.598-190G>T
XM_006712496.1:c.364-190G>T XP_006712559.1:n.364-190G>T
XM_017003988.2:c.505-190G>T XP_016859477.1:n.505-190G>T
NM_000576.3:c.598-190G>T MANE Select NP_000567.1:n.598-190G>T
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