Canonical Allele Identifier: CA1595018354
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322815G= , CM000667.2:g.159322815G= GRCh38
NC_000005.9:g.158749823G= , CM000667.1:g.158749823G= GRCh37
NC_000005.8:g.158682401G= NCBI36
NG_009618.1:g.12659C= , LRG_71:g.12659C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2295C= ENSP00000512849.1:n.-148-2295C=
ENST00000696751.1:c.364+239C= ENSP00000512850.1:n.364+239C=
ENST00000231228.3:c.364+239C= MANE Select ENSP00000231228.2:n.364+239C=
ENST00000231228.2:c.364+239C= ENSP00000231228.2:n.364+239C=
NM_002187.2:c.364+239C= , LRG_71t1:c.364+239C= NP_002178.2:n.364+239C=
XR_001742945.1:n.147+2219G=
NM_002187.3:c.364+239C= MANE Select NP_002178.2:n.364+239C=
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