Canonical Allele Identifier: CA362032995
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159320494-C-T
MyVariant Identifiers: chr5:g.158747502C>T (hg19) chr5:g.159320494C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320494C>T , CM000667.2:g.159320494C>T GRCh38
NC_000005.9:g.158747502C>T , CM000667.1:g.158747502C>T GRCh37
NC_000005.8:g.158680080C>T NCBI36
NG_009618.1:g.14980G>A , LRG_71:g.14980G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-122G>A ENSP00000512849.1:n.-122G>A
ENST00000696751.1:c.*4G>A ENSP00000512850.1:n.*4G>A
ENST00000231228.3:c.509G>A MANE Select ENSP00000231228.2:p.Cys170Tyr
ENST00000231228.2:c.509G>A ENSP00000231228.2:p.Cys170Tyr
NM_002187.2:c.509G>A , LRG_71t1:c.509G>A NP_002178.2:p.Cys170Tyr
XR_001742945.1:n.45C>T
NM_002187.3:c.509G>A MANE Select NP_002178.2:p.Cys170Tyr
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