Canonical Allele Identifier: CA1595017289
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320411C= , CM000667.2:g.159320411C= GRCh38
NC_000005.9:g.158747419C= , CM000667.1:g.158747419C= GRCh37
NC_000005.8:g.158679997C= NCBI36
NG_009618.1:g.15063G= , LRG_71:g.15063G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-39G= ENSP00000512849.1:n.-39G=
ENST00000696751.1:c.*87G= ENSP00000512850.1:n.*87G=
ENST00000231228.3:c.592G= MANE Select ENSP00000231228.2:p.Ala198=
ENST00000231228.2:c.592G= ENSP00000231228.2:p.Ala198=
NM_002187.2:c.592G= , LRG_71t1:c.592G= NP_002178.2:p.Ala198=
NM_002187.3:c.592G= MANE Select NP_002178.2:p.Ala198=