Canonical Allele Identifier: CA1595018578

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323292A= , CM000667.2:g.159323292A=	GRCh38
NC_000005.9:g.158750300A= , CM000667.1:g.158750300A=	GRCh37
NC_000005.8:g.158682878A=	NCBI36
NG_009618.1:g.12182T= , LRG_71:g.12182T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2772T=	ENSP00000512849.1:n.-148-2772T=
ENST00000696751.1:c.126T=	ENSP00000512850.1:p.Pro42=
ENST00000231228.3:c.126T= MANE Select	ENSP00000231228.2:p.Pro42=
ENST00000231228.2:c.126T=	ENSP00000231228.2:p.Pro42=
NM_002187.2:c.126T= , LRG_71t1:c.126T=	NP_002178.2:p.Pro42=
XR_001742945.1:n.148-2242A=
NM_002187.3:c.126T= MANE Select	NP_002178.2:p.Pro42=