Canonical Allele Identifier: CA1595017285
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320394C= , CM000667.2:g.159320394C= GRCh38
NC_000005.9:g.158747402C= , CM000667.1:g.158747402C= GRCh37
NC_000005.8:g.158679980C= NCBI36
NG_009618.1:g.15080G= , LRG_71:g.15080G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-22G= ENSP00000512849.1:n.-22G=
ENST00000696751.1:c.*104G= ENSP00000512850.1:n.*104G=
ENST00000231228.3:c.609G= MANE Select ENSP00000231228.2:p.Glu203=
ENST00000231228.2:c.609G= ENSP00000231228.2:p.Glu203=
NM_002187.2:c.609G= , LRG_71t1:c.609G= NP_002178.2:p.Glu203=
NM_002187.3:c.609G= MANE Select NP_002178.2:p.Glu203=