Canonical Allele Identifier: CA535595897
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1276943551
gnomAD v2: 2-113588226-G-A
gnomAD v3: 2-112830649-G-A
gnomAD v4: 2-112830649-G-A
MyVariant Identifiers: chr2:g.113588226G>A (hg19) chr2:g.112830649G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830649G>A , CM000664.2:g.112830649G>A GRCh38
NC_000002.11:g.113588226G>A , CM000664.1:g.113588226G>A GRCh37
NC_000002.10:g.113304697G>A NCBI36
NG_008851.1:g.11131C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.598-76C>T MANE Select ENSP00000263341.2:n.598-76C>T
ENST00000263341.6:c.598-76C>T ENSP00000263341.2:n.598-76C>T
ENST00000491056.5:n.1405-76C>T
NM_000576.2:c.598-76C>T NP_000567.1:n.598-76C>T
XM_006712496.1:c.364-76C>T XP_006712559.1:n.364-76C>T
XM_017003988.2:c.505-76C>T XP_016859477.1:n.505-76C>T
NM_000576.3:c.598-76C>T MANE Select NP_000567.1:n.598-76C>T
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