Canonical Allele Identifier: CA1595017287
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320402C= , CM000667.2:g.159320402C= GRCh38
NC_000005.9:g.158747410C= , CM000667.1:g.158747410C= GRCh37
NC_000005.8:g.158679988C= NCBI36
NG_009618.1:g.15072G= , LRG_71:g.15072G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-30G= ENSP00000512849.1:n.-30G=
ENST00000696751.1:c.*96G= ENSP00000512850.1:n.*96G=
ENST00000231228.3:c.601G= MANE Select ENSP00000231228.2:p.Ala201=
ENST00000231228.2:c.601G= ENSP00000231228.2:p.Ala201=
NM_002187.2:c.601G= , LRG_71t1:c.601G= NP_002178.2:p.Ala201=
NM_002187.3:c.601G= MANE Select NP_002178.2:p.Ala201=