Canonical Allele Identifier: CA1595017305
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320444A= , CM000667.2:g.159320444A= GRCh38
NC_000005.9:g.158747452A= , CM000667.1:g.158747452A= GRCh37
NC_000005.8:g.158680030A= NCBI36
NG_009618.1:g.15030T= , LRG_71:g.15030T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-72T= ENSP00000512849.1:n.-72T=
ENST00000696751.1:c.*54T= ENSP00000512850.1:n.*54T=
ENST00000231228.3:c.559T= MANE Select ENSP00000231228.2:p.Tyr187=
ENST00000231228.2:c.559T= ENSP00000231228.2:p.Tyr187=
NM_002187.2:c.559T= , LRG_71t1:c.559T= NP_002178.2:p.Tyr187=
NM_002187.3:c.559T= MANE Select NP_002178.2:p.Tyr187=