Canonical Allele Identifier: CA1595017968

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321857C= , CM000667.2:g.159321857C=	GRCh38
NC_000005.9:g.158748865C= , CM000667.1:g.158748865C=	GRCh37
NC_000005.8:g.158681443C=	NCBI36
NG_009618.1:g.13617G= , LRG_71:g.13617G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1337G=	ENSP00000512849.1:n.-148-1337G=
ENST00000696751.1:c.364+1197G=	ENSP00000512850.1:n.364+1197G=
ENST00000231228.3:c.482+537G= MANE Select	ENSP00000231228.2:n.482+537G=
ENST00000231228.2:c.482+537G=	ENSP00000231228.2:n.482+537G=
NM_002187.2:c.482+537G= , LRG_71t1:c.482+537G=	NP_002178.2:n.482+537G=
XR_001742945.1:n.147+1261C=
NM_002187.3:c.482+537G= MANE Select	NP_002178.2:n.482+537G=