Canonical Allele Identifier: CA1595017329
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320509G= , CM000667.2:g.159320509G= GRCh38
NC_000005.9:g.158747517G= , CM000667.1:g.158747517G= GRCh37
NC_000005.8:g.158680095G= NCBI36
NG_009618.1:g.14965C= , LRG_71:g.14965C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-137C= ENSP00000512849.1:n.-137C=
ENST00000696751.1:c.376C= ENSP00000512850.1:p.Pro126=
ENST00000231228.3:c.494C= MANE Select ENSP00000231228.2:p.Pro165=
ENST00000231228.2:c.494C= ENSP00000231228.2:p.Pro165=
NM_002187.2:c.494C= , LRG_71t1:c.494C= NP_002178.2:p.Pro165=
XR_001742945.1:n.60G=
NM_002187.3:c.494C= MANE Select NP_002178.2:p.Pro165=