Canonical Allele Identifier: CA1595045700
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316007_159316008delinsAG , CM000667.2:g.159316007_159316008delinsAG GRCh38
NC_000005.9:g.158743015_158743016delinsAG , CM000667.1:g.158743015_158743016delinsAG GRCh37
NC_000005.8:g.158675593_158675594delinsAG NCBI36
NG_009618.1:g.19466_19467delinsCT , LRG_71:g.19466_19467delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*93_*94delinsCT ENSP00000512849.1:n.*93_*94delinsCT
ENST00000696751.1:c.*575_*576delinsCT ENSP00000512850.1:n.*575_*576delinsCT
ENST00000231228.3:c.*93_*94delinsCT MANE Select ENSP00000231228.2:n.*93_*94delinsCT
ENST00000231228.2:c.*93_*94delinsCT ENSP00000231228.2:n.*93_*94delinsCT
NM_002187.2:c.*93_*94delinsCT , LRG_71t1:c.*93_*94delinsCT NP_002178.2:n.*93_*94delinsCT
NM_002187.3:c.*93_*94delinsCT MANE Select NP_002178.2:n.*93_*94delinsCT