Canonical Allele Identifier: CA1595017301
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320434G= , CM000667.2:g.159320434G= GRCh38
NC_000005.9:g.158747442G= , CM000667.1:g.158747442G= GRCh37
NC_000005.8:g.158680020G= NCBI36
NG_009618.1:g.15040C= , LRG_71:g.15040C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-62C= ENSP00000512849.1:n.-62C=
ENST00000696751.1:c.*64C= ENSP00000512850.1:n.*64C=
ENST00000231228.3:c.569C= MANE Select ENSP00000231228.2:p.Ser190=
ENST00000231228.2:c.569C= ENSP00000231228.2:p.Ser190=
NM_002187.2:c.569C= , LRG_71t1:c.569C= NP_002178.2:p.Ser190=
NM_002187.3:c.569C= MANE Select NP_002178.2:p.Ser190=