Canonical Allele Identifier: CA1595045779

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316206A= , CM000667.2:g.159316206A=	GRCh38
NC_000005.9:g.158743214A= , CM000667.1:g.158743214A=	GRCh37
NC_000005.8:g.158675792A=	NCBI36
NG_009618.1:g.19268T= , LRG_71:g.19268T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1-106T=	ENSP00000512849.1:n.*1-106T=
ENST00000696751.1:c.*483-106T=	ENSP00000512850.1:n.*483-106T=
ENST00000231228.3:c.*1-106T= MANE Select	ENSP00000231228.2:n.*1-106T=
ENST00000231228.2:c.*1-106T=	ENSP00000231228.2:n.*1-106T=
NM_002187.2:c.*1-106T= , LRG_71t1:c.*1-106T=	NP_002178.2:n.*1-106T=
NM_002187.3:c.*1-106T= MANE Select	NP_002178.2:n.*1-106T=