Canonical Allele Identifier: CA1595020148
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327163A= , CM000667.2:g.159327163A= GRCh38
NC_000005.9:g.158754171A= , CM000667.1:g.158754171A= GRCh37
NC_000005.8:g.158686749A= NCBI36
NG_009618.1:g.8311T= , LRG_71:g.8311T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3269T= ENSP00000512849.1:n.-149+3269T=
ENST00000696751.1:c.1-381T= ENSP00000512850.1:n.1-381T=
ENST00000696752.1:n.433-381T=
ENST00000231228.3:c.1-381T= MANE Select ENSP00000231228.2:n.1-381T=
ENST00000231228.2:c.1-381T= ENSP00000231228.2:n.1-381T=
NM_002187.2:c.1-381T= , LRG_71t1:c.1-381T= NP_002178.2:n.1-381T=
NM_002187.3:c.1-381T= MANE Select NP_002178.2:n.1-381T=