Canonical Allele Identifier: CA348287024
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs1242592899
MyVariant Identifiers: chr2:g.113588128G>C (hg19) chr2:g.112830551G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830551G>C , CM000664.2:g.112830551G>C GRCh38
NC_000002.11:g.113588128G>C , CM000664.1:g.113588128G>C GRCh37
NC_000002.10:g.113304599G>C NCBI36
NG_008851.1:g.11229C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263341.7:c.620C>G MANE Select ENSP00000263341.2:p.Pro207Arg
ENST00000263341.6:c.620C>G ENSP00000263341.2:p.Pro207Arg
ENST00000491056.5:n.1427C>G
NM_000576.2:c.620C>G NP_000567.1:p.Pro207Arg
XM_006712496.1:c.386C>G XP_006712559.1:p.Pro129Arg
XM_017003988.2:c.527C>G XP_016859477.1:p.Pro176Arg
NM_000576.3:c.620C>G MANE Select NP_000567.1:p.Pro207Arg
Search 100 bp 5'
Search 100 bp 3'