Canonical Allele Identifier: CA447681173
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158750138A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323130A>T , CM000667.2:g.159323130A>T GRCh38
NC_000005.9:g.158750138A>T , CM000667.1:g.158750138A>T GRCh37
NC_000005.8:g.158682716A>T NCBI36
NG_009618.1:g.12344T>A , LRG_71:g.12344T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2610T>A ENSP00000512849.1:n.-148-2610T>A
ENST00000696751.1:c.288T>A ENSP00000512850.1:p.Val96=
ENST00000231228.3:c.288T>A MANE Select ENSP00000231228.2:p.Val96=
ENST00000231228.2:c.288T>A ENSP00000231228.2:p.Val96=
NM_002187.2:c.288T>A , LRG_71t1:c.288T>A NP_002178.2:p.Val96=
XR_001742945.1:n.148-2404A>T
NM_002187.3:c.288T>A MANE Select NP_002178.2:p.Val96=
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