Canonical Allele Identifier: CA1595017145

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320084C= , CM000667.2:g.159320084C=	GRCh38
NC_000005.9:g.158747092C= , CM000667.1:g.158747092C=	GRCh37
NC_000005.8:g.158679670C=	NCBI36
NG_009618.1:g.15390G= , LRG_71:g.15390G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+222G=	ENSP00000512849.1:n.67+222G=
ENST00000696751.1:c.*192+222G=	ENSP00000512850.1:n.*192+222G=
ENST00000231228.3:c.697+222G= MANE Select	ENSP00000231228.2:n.697+222G=
ENST00000231228.2:c.697+222G=	ENSP00000231228.2:n.697+222G=
NM_002187.2:c.697+222G= , LRG_71t1:c.697+222G=	NP_002178.2:n.697+222G=
NM_002187.3:c.697+222G= MANE Select	NP_002178.2:n.697+222G=