Canonical Allele Identifier: CA1595020723
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159328531C= , CM000667.2:g.159328531C= GRCh38
NC_000005.9:g.158755539C= , CM000667.1:g.158755539C= GRCh37
NC_000005.8:g.158688117C= NCBI36
NG_009618.1:g.6943G= , LRG_71:g.6943G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+1901G= ENSP00000512849.1:n.-149+1901G=
ENST00000696751.1:c.1-1749G= ENSP00000512850.1:n.1-1749G=
ENST00000696752.1:n.433-1749G=
ENST00000231228.3:c.1-1749G= MANE Select ENSP00000231228.2:n.1-1749G=
ENST00000231228.2:c.1-1749G= ENSP00000231228.2:n.1-1749G=
NM_002187.2:c.1-1749G= , LRG_71t1:c.1-1749G= NP_002178.2:n.1-1749G=
NM_002187.3:c.1-1749G= MANE Select NP_002178.2:n.1-1749G=