Canonical Allele Identifier: CA1595018484
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323106A= , CM000667.2:g.159323106A= GRCh38
NC_000005.9:g.158750114A= , CM000667.1:g.158750114A= GRCh37
NC_000005.8:g.158682692A= NCBI36
NG_009618.1:g.12368T= , LRG_71:g.12368T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2586T= ENSP00000512849.1:n.-148-2586T=
ENST00000696751.1:c.312T= ENSP00000512850.1:p.Leu104=
ENST00000231228.3:c.312T= MANE Select ENSP00000231228.2:p.Leu104=
ENST00000231228.2:c.312T= ENSP00000231228.2:p.Leu104=
NM_002187.2:c.312T= , LRG_71t1:c.312T= NP_002178.2:p.Leu104=
XR_001742945.1:n.148-2428A=
NM_002187.3:c.312T= MANE Select NP_002178.2:p.Leu104=