Canonical Allele Identifier: CA1279938271
Gene: IL1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112830745_112830748delinsCCTT , CM000664.2:g.112830745_112830748delinsCCTT GRCh38
NC_000002.11:g.113588322_113588325delinsCCTT , CM000664.1:g.113588322_113588325delinsCCTT GRCh37
NC_000002.10:g.113304793_113304796delinsCCTT NCBI36
NG_008851.1:g.11032_11035delinsAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.598-175_598-172delinsAAGG MANE Select ENSP00000263341.2:n.598-175_598-172delinsAAGG
ENST00000263341.6:c.598-175_598-172delinsAAGG ENSP00000263341.2:n.598-175_598-172delinsAAGG
ENST00000491056.5:n.1405-175_1405-172delinsAAGG
NM_000576.2:c.598-175_598-172delinsAAGG NP_000567.1:n.598-175_598-172delinsAAGG
XM_006712496.1:c.364-175_364-172delinsAAGG XP_006712559.1:n.364-175_364-172delinsAAGG
XM_017003988.2:c.505-175_505-172delinsAAGG XP_016859477.1:n.505-175_505-172delinsAAGG
NM_000576.3:c.598-175_598-172delinsAAGG MANE Select NP_000567.1:n.598-175_598-172delinsAAGG
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