Canonical Allele Identifier: CA1595017333

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320518G= , CM000667.2:g.159320518G=	GRCh38
NC_000005.9:g.158747526G= , CM000667.1:g.158747526G=	GRCh37
NC_000005.8:g.158680104G=	NCBI36
NG_009618.1:g.14956C= , LRG_71:g.14956C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-146C=	ENSP00000512849.1:n.-146C=
ENST00000696751.1:c.367C=	ENSP00000512850.1:p.Leu123=
ENST00000231228.3:c.485C= MANE Select	ENSP00000231228.2:p.Ser162=
ENST00000231228.2:c.485C=	ENSP00000231228.2:p.Ser162=
NM_002187.2:c.485C= , LRG_71t1:c.485C=	NP_002178.2:p.Ser162=
XR_001742945.1:n.69G=
NM_002187.3:c.485C= MANE Select	NP_002178.2:p.Ser162=