Canonical Allele Identifier: CA1595017348
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320557T= , CM000667.2:g.159320557T= GRCh38
NC_000005.9:g.158747565T= , CM000667.1:g.158747565T= GRCh37
NC_000005.8:g.158680143T= NCBI36
NG_009618.1:g.14917A= , LRG_71:g.14917A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-37A= ENSP00000512849.1:n.-148-37A=
ENST00000696751.1:c.365-37A= ENSP00000512850.1:n.365-37A=
ENST00000231228.3:c.483-37A= MANE Select ENSP00000231228.2:n.483-37A=
ENST00000231228.2:c.483-37A= ENSP00000231228.2:n.483-37A=
NM_002187.2:c.483-37A= , LRG_71t1:c.483-37A= NP_002178.2:n.483-37A=
XR_001742945.1:n.108T=
NM_002187.3:c.483-37A= MANE Select NP_002178.2:n.483-37A=