Canonical Allele Identifier: CA1595045670
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315942T= , CM000667.2:g.159315942T= GRCh38
NC_000005.9:g.158742950T= , CM000667.1:g.158742950T= GRCh37
NC_000005.8:g.158675528T= NCBI36
NG_009618.1:g.19532A= , LRG_71:g.19532A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*159A= ENSP00000512849.1:n.*159A=
ENST00000696751.1:c.*641A= ENSP00000512850.1:n.*641A=
ENST00000231228.3:c.*159A= MANE Select ENSP00000231228.2:n.*159A=
ENST00000231228.2:c.*159A= ENSP00000231228.2:n.*159A=
NM_002187.2:c.*159A= , LRG_71t1:c.*159A= NP_002178.2:n.*159A=
NM_002187.3:c.*159A= MANE Select NP_002178.2:n.*159A=