Canonical Allele Identifier: CA1595020998

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159329184_159329188delinsTTTTG , CM000667.2:g.159329184_159329188delinsTTTTG	GRCh38
NC_000005.9:g.158756192_158756196delinsTTTTG , CM000667.1:g.158756192_158756196delinsTTTTG	GRCh37
NC_000005.8:g.158688770_158688774delinsTTTTG	NCBI36
NG_009618.1:g.6286_6290delinsCAAAA , LRG_71:g.6286_6290delinsCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1244_-149+1248delinsCAAAA	ENSP00000512849.1:n.-149+1244_-149+1248delinsCAAAA
ENST00000696751.1:c.-1+1244_-1+1248delinsCAAAA	ENSP00000512850.1:n.-1+1244_-1+1248delinsCAAAA
ENST00000696752.1:n.432+1244_432+1248delinsCAAAA
ENST00000231228.3:c.-1+1244_-1+1248delinsCAAAA MANE Select	ENSP00000231228.2:n.-1+1244_-1+1248delinsCAAAA
ENST00000231228.2:c.-1+1244_-1+1248delinsCAAAA	ENSP00000231228.2:n.-1+1244_-1+1248delinsCAAAA
NM_002187.2:c.-1+1244_-1+1248delinsCAAAA , LRG_71t1:c.-1+1244_-1+1248delinsCAAAA	NP_002178.2:n.-1+1244_-1+1248delinsCAAAA
NM_002187.3:c.-1+1244_-1+1248delinsCAAAA MANE Select	NP_002178.2:n.-1+1244_-1+1248delinsCAAAA