Canonical Allele Identifier: CA1595020834

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328815_159328816delinsAC , CM000667.2:g.159328815_159328816delinsAC	GRCh38
NC_000005.9:g.158755823_158755824delinsAC , CM000667.1:g.158755823_158755824delinsAC	GRCh37
NC_000005.8:g.158688401_158688402delinsAC	NCBI36
NG_009618.1:g.6658_6659delinsGT , LRG_71:g.6658_6659delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1616_-149+1617delinsGT	ENSP00000512849.1:n.-149+1616_-149+1617delinsGT
ENST00000696751.1:c.-1+1616_-1+1617delinsGT	ENSP00000512850.1:n.-1+1616_-1+1617delinsGT
ENST00000696752.1:n.432+1616_432+1617delinsGT
ENST00000231228.3:c.-1+1616_-1+1617delinsGT MANE Select	ENSP00000231228.2:n.-1+1616_-1+1617delinsGT
ENST00000231228.2:c.-1+1616_-1+1617delinsGT	ENSP00000231228.2:n.-1+1616_-1+1617delinsGT
NM_002187.2:c.-1+1616_-1+1617delinsGT , LRG_71t1:c.-1+1616_-1+1617delinsGT	NP_002178.2:n.-1+1616_-1+1617delinsGT
NM_002187.3:c.-1+1616_-1+1617delinsGT MANE Select	NP_002178.2:n.-1+1616_-1+1617delinsGT