Canonical Allele Identifier: CA1595020951
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159329084C= , CM000667.2:g.159329084C= GRCh38
NC_000005.9:g.158756092C= , CM000667.1:g.158756092C= GRCh37
NC_000005.8:g.158688670C= NCBI36
NG_009618.1:g.6390G= , LRG_71:g.6390G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+1348G= ENSP00000512849.1:n.-149+1348G=
ENST00000696751.1:c.-1+1348G= ENSP00000512850.1:n.-1+1348G=
ENST00000696752.1:n.432+1348G=
ENST00000231228.3:c.-1+1348G= MANE Select ENSP00000231228.2:n.-1+1348G=
ENST00000231228.2:c.-1+1348G= ENSP00000231228.2:n.-1+1348G=
NM_002187.2:c.-1+1348G= , LRG_71t1:c.-1+1348G= NP_002178.2:n.-1+1348G=
NM_002187.3:c.-1+1348G= MANE Select NP_002178.2:n.-1+1348G=