Canonical Allele Identifier: CA2676265390
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323459-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323459T>A , CM000667.2:g.159323459T>A GRCh38
NC_000005.9:g.158750467T>A , CM000667.1:g.158750467T>A GRCh37
NC_000005.8:g.158683045T>A NCBI36
NG_009618.1:g.12015A>T , LRG_71:g.12015A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2939A>T ENSP00000512849.1:n.-148-2939A>T
ENST00000696751.1:c.89-130A>T ENSP00000512850.1:n.89-130A>T
ENST00000231228.3:c.89-130A>T MANE Select ENSP00000231228.2:n.89-130A>T
ENST00000231228.2:c.89-130A>T ENSP00000231228.2:n.89-130A>T
NM_002187.2:c.89-130A>T , LRG_71t1:c.89-130A>T NP_002178.2:n.89-130A>T
XR_001742945.1:n.148-2075T>A
NM_002187.3:c.89-130A>T MANE Select NP_002178.2:n.89-130A>T
Search 100 bp 5'
Search 100 bp 3'