Canonical Allele Identifier: CA53696398
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs995863985
gnomAD v3: 2-112830652-A-G
gnomAD v4: 2-112830652-A-G
MyVariant Identifiers: chr2:g.113588229A>G (hg19) chr2:g.112830652A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830652A>G , CM000664.2:g.112830652A>G GRCh38
NC_000002.11:g.113588229A>G , CM000664.1:g.113588229A>G GRCh37
NC_000002.10:g.113304700A>G NCBI36
NG_008851.1:g.11128T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.598-79T>C MANE Select ENSP00000263341.2:n.598-79T>C
ENST00000263341.6:c.598-79T>C ENSP00000263341.2:n.598-79T>C
ENST00000491056.5:n.1405-79T>C
NM_000576.2:c.598-79T>C NP_000567.1:n.598-79T>C
XM_006712496.1:c.364-79T>C XP_006712559.1:n.364-79T>C
XM_017003988.2:c.505-79T>C XP_016859477.1:n.505-79T>C
NM_000576.3:c.598-79T>C MANE Select NP_000567.1:n.598-79T>C
Search 100 bp 5'
Search 100 bp 3'