Canonical Allele Identifier: CA2769108159

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321960A>T , CM000667.2:g.159321960A>T	GRCh38
NC_000005.9:g.158748968A>T , CM000667.1:g.158748968A>T	GRCh37
NC_000005.8:g.158681546A>T	NCBI36
NG_009618.1:g.13514T>A , LRG_71:g.13514T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1440T>A	ENSP00000512849.1:n.-148-1440T>A
ENST00000696751.1:c.364+1094T>A	ENSP00000512850.1:n.364+1094T>A
ENST00000231228.3:c.482+434T>A MANE Select	ENSP00000231228.2:n.482+434T>A
ENST00000231228.2:c.482+434T>A	ENSP00000231228.2:n.482+434T>A
NM_002187.2:c.482+434T>A , LRG_71t1:c.482+434T>A	NP_002178.2:n.482+434T>A
XR_001742945.1:n.147+1364A>T
NM_002187.3:c.482+434T>A MANE Select	NP_002178.2:n.482+434T>A