Canonical Allele Identifier: CA1595045225
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315007G= , CM000667.2:g.159315007G= GRCh38
NC_000005.9:g.158742015G= , CM000667.1:g.158742015G= GRCh37
NC_000005.8:g.158674593G= NCBI36
NG_009618.1:g.20467C= , LRG_71:g.20467C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1094C= ENSP00000512849.1:n.*1094C=
ENST00000696751.1:c.*1576C= ENSP00000512850.1:n.*1576C=
ENST00000231228.3:c.*1094C= MANE Select ENSP00000231228.2:n.*1094C=
ENST00000231228.2:c.*1094C= ENSP00000231228.2:n.*1094C=
NM_002187.2:c.*1094C= , LRG_71t1:c.*1094C= NP_002178.2:n.*1094C=
XR_941138.1:n.364-211G=
XR_941138.2:n.431-211G=
NM_002187.3:c.*1094C= MANE Select NP_002178.2:n.*1094C=