Canonical Allele Identifier: CA1595020848
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159328831T= , CM000667.2:g.159328831T= GRCh38
NC_000005.9:g.158755839T= , CM000667.1:g.158755839T= GRCh37
NC_000005.8:g.158688417T= NCBI36
NG_009618.1:g.6643A= , LRG_71:g.6643A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+1601A= ENSP00000512849.1:n.-149+1601A=
ENST00000696751.1:c.-1+1601A= ENSP00000512850.1:n.-1+1601A=
ENST00000696752.1:n.432+1601A=
ENST00000231228.3:c.-1+1601A= MANE Select ENSP00000231228.2:n.-1+1601A=
ENST00000231228.2:c.-1+1601A= ENSP00000231228.2:n.-1+1601A=
NM_002187.2:c.-1+1601A= , LRG_71t1:c.-1+1601A= NP_002178.2:n.-1+1601A=
NM_002187.3:c.-1+1601A= MANE Select NP_002178.2:n.-1+1601A=