Canonical Allele Identifier: CA1595017319

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320492C= , CM000667.2:g.159320492C=	GRCh38
NC_000005.9:g.158747500C= , CM000667.1:g.158747500C=	GRCh37
NC_000005.8:g.158680078C=	NCBI36
NG_009618.1:g.14982G= , LRG_71:g.14982G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-120G=	ENSP00000512849.1:n.-120G=
ENST00000696751.1:c.*6G=	ENSP00000512850.1:n.*6G=
ENST00000231228.3:c.511G= MANE Select	ENSP00000231228.2:p.Gly171=
ENST00000231228.2:c.511G=	ENSP00000231228.2:p.Gly171=
NM_002187.2:c.511G= , LRG_71t1:c.511G=	NP_002178.2:p.Gly171=
XR_001742945.1:n.43C=
NM_002187.3:c.511G= MANE Select	NP_002178.2:p.Gly171=