Canonical Allele Identifier: CA1595017277
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320378C= , CM000667.2:g.159320378C= GRCh38
NC_000005.9:g.158747386C= , CM000667.1:g.158747386C= GRCh37
NC_000005.8:g.158679964C= NCBI36
NG_009618.1:g.15096G= , LRG_71:g.15096G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-6G= ENSP00000512849.1:n.-6G=
ENST00000696751.1:c.*120G= ENSP00000512850.1:n.*120G=
ENST00000231228.3:c.625G= MANE Select ENSP00000231228.2:p.Glu209=
ENST00000231228.2:c.625G= ENSP00000231228.2:p.Glu209=
NM_002187.2:c.625G= , LRG_71t1:c.625G= NP_002178.2:p.Glu209=
NM_002187.3:c.625G= MANE Select NP_002178.2:p.Glu209=