Canonical Allele Identifier: CA362035955
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323182A>T , CM000667.2:g.159323182A>T GRCh38
NC_000005.9:g.158750190A>T , CM000667.1:g.158750190A>T GRCh37
NC_000005.8:g.158682768A>T NCBI36
NG_009618.1:g.12292T>A , LRG_71:g.12292T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2662T>A ENSP00000512849.1:n.-148-2662T>A
ENST00000696751.1:c.236T>A ENSP00000512850.1:p.Val79Asp
ENST00000231228.3:c.236T>A MANE Select ENSP00000231228.2:p.Val79Asp
ENST00000231228.2:c.236T>A ENSP00000231228.2:p.Val79Asp
NM_002187.2:c.236T>A , LRG_71t1:c.236T>A NP_002178.2:p.Val79Asp
XR_001742945.1:n.148-2352A>T
NM_002187.3:c.236T>A MANE Select NP_002178.2:p.Val79Asp