Canonical Allele Identifier: CA1595017283
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320389C= , CM000667.2:g.159320389C= GRCh38
NC_000005.9:g.158747397C= , CM000667.1:g.158747397C= GRCh37
NC_000005.8:g.158679975C= NCBI36
NG_009618.1:g.15085G= , LRG_71:g.15085G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-17G= ENSP00000512849.1:n.-17G=
ENST00000696751.1:c.*109G= ENSP00000512850.1:n.*109G=
ENST00000231228.3:c.614G= MANE Select ENSP00000231228.2:p.Ser205=
ENST00000231228.2:c.614G= ENSP00000231228.2:p.Ser205=
NM_002187.2:c.614G= , LRG_71t1:c.614G= NP_002178.2:p.Ser205=
NM_002187.3:c.614G= MANE Select NP_002178.2:p.Ser205=