Canonical Allele Identifier: CA1595017269

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320362G= , CM000667.2:g.159320362G=	GRCh38
NC_000005.9:g.158747370G= , CM000667.1:g.158747370G=	GRCh37
NC_000005.8:g.158679948G=	NCBI36
NG_009618.1:g.15112C= , LRG_71:g.15112C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.11C=	ENSP00000512849.1:p.Ala4=
ENST00000696751.1:c.*136C=	ENSP00000512850.1:n.*136C=
ENST00000231228.3:c.641C= MANE Select	ENSP00000231228.2:p.Ala214=
ENST00000231228.2:c.641C=	ENSP00000231228.2:p.Ala214=
NM_002187.2:c.641C= , LRG_71t1:c.641C=	NP_002178.2:p.Ala214=
NM_002187.3:c.641C= MANE Select	NP_002178.2:p.Ala214=