Canonical Allele Identifier: CA1595020912

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328989_159328991delinsTGA , CM000667.2:g.159328989_159328991delinsTGA	GRCh38
NC_000005.9:g.158755997_158755999delinsTGA , CM000667.1:g.158755997_158755999delinsTGA	GRCh37
NC_000005.8:g.158688575_158688577delinsTGA	NCBI36
NG_009618.1:g.6483_6485delinsTCA , LRG_71:g.6483_6485delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1441_-149+1443delinsTCA	ENSP00000512849.1:n.-149+1441_-149+1443delinsTCA
ENST00000696751.1:c.-1+1441_-1+1443delinsTCA	ENSP00000512850.1:n.-1+1441_-1+1443delinsTCA
ENST00000696752.1:n.432+1441_432+1443delinsTCA
ENST00000231228.3:c.-1+1441_-1+1443delinsTCA MANE Select	ENSP00000231228.2:n.-1+1441_-1+1443delinsTCA
ENST00000231228.2:c.-1+1441_-1+1443delinsTCA	ENSP00000231228.2:n.-1+1441_-1+1443delinsTCA
NM_002187.2:c.-1+1441_-1+1443delinsTCA , LRG_71t1:c.-1+1441_-1+1443delinsTCA	NP_002178.2:n.-1+1441_-1+1443delinsTCA
NM_002187.3:c.-1+1441_-1+1443delinsTCA MANE Select	NP_002178.2:n.-1+1441_-1+1443delinsTCA