Canonical Allele Identifier: CA2519072357
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315038A>T , CM000667.2:g.159315038A>T GRCh38
NC_000005.9:g.158742046A>T , CM000667.1:g.158742046A>T GRCh37
NC_000005.8:g.158674624A>T NCBI36
NG_009618.1:g.20436T>A , LRG_71:g.20436T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1063T>A ENSP00000512849.1:n.*1063T>A
ENST00000696751.1:c.*1545T>A ENSP00000512850.1:n.*1545T>A
ENST00000231228.3:c.*1063T>A MANE Select ENSP00000231228.2:n.*1063T>A
ENST00000231228.2:c.*1063T>A ENSP00000231228.2:n.*1063T>A
NM_002187.2:c.*1063T>A , LRG_71t1:c.*1063T>A NP_002178.2:n.*1063T>A
XR_941138.1:n.364-180A>T
XR_941138.2:n.431-180A>T
NM_002187.3:c.*1063T>A MANE Select NP_002178.2:n.*1063T>A
Search 100 bp 5'
Search 100 bp 3'