Canonical Allele Identifier: CA362033038
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158747523G>T (hg19) chr5:g.159320515G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320515G>T , CM000667.2:g.159320515G>T GRCh38
NC_000005.9:g.158747523G>T , CM000667.1:g.158747523G>T GRCh37
NC_000005.8:g.158680101G>T NCBI36
NG_009618.1:g.14959C>A , LRG_71:g.14959C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-143C>A ENSP00000512849.1:n.-143C>A
ENST00000696751.1:c.370C>A ENSP00000512850.1:p.Leu124Met
ENST00000231228.3:c.488C>A MANE Select ENSP00000231228.2:p.Ser163Tyr
ENST00000231228.2:c.488C>A ENSP00000231228.2:p.Ser163Tyr
NM_002187.2:c.488C>A , LRG_71t1:c.488C>A NP_002178.2:p.Ser163Tyr
XR_001742945.1:n.66G>T
NM_002187.3:c.488C>A MANE Select NP_002178.2:p.Ser163Tyr
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