Canonical Allele Identifier: CA1595017274
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320373G= , CM000667.2:g.159320373G= GRCh38
NC_000005.9:g.158747381G= , CM000667.1:g.158747381G= GRCh37
NC_000005.8:g.158679959G= NCBI36
NG_009618.1:g.15101C= , LRG_71:g.15101C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-1C= ENSP00000512849.1:n.-1C=
ENST00000696751.1:c.*125C= ENSP00000512850.1:n.*125C=
ENST00000231228.3:c.630C= MANE Select ENSP00000231228.2:p.Val210=
ENST00000231228.2:c.630C= ENSP00000231228.2:p.Val210=
NM_002187.2:c.630C= , LRG_71t1:c.630C= NP_002178.2:p.Val210=
NM_002187.3:c.630C= MANE Select NP_002178.2:p.Val210=