Canonical Allele Identifier: CA1595018567
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323269C= , CM000667.2:g.159323269C= GRCh38
NC_000005.9:g.158750277C= , CM000667.1:g.158750277C= GRCh37
NC_000005.8:g.158682855C= NCBI36
NG_009618.1:g.12205G= , LRG_71:g.12205G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2749G= ENSP00000512849.1:n.-148-2749G=
ENST00000696751.1:c.149G= ENSP00000512850.1:p.Cys50=
ENST00000231228.3:c.149G= MANE Select ENSP00000231228.2:p.Cys50=
ENST00000231228.2:c.149G= ENSP00000231228.2:p.Cys50=
NM_002187.2:c.149G= , LRG_71t1:c.149G= NP_002178.2:p.Cys50=
XR_001742945.1:n.148-2265C=
NM_002187.3:c.149G= MANE Select NP_002178.2:p.Cys50=