Canonical Allele Identifier: CA1595018097
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322185C= , CM000667.2:g.159322185C= GRCh38
NC_000005.9:g.158749193C= , CM000667.1:g.158749193C= GRCh37
NC_000005.8:g.158681771C= NCBI36
NG_009618.1:g.13289G= , LRG_71:g.13289G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-1665G= ENSP00000512849.1:n.-148-1665G=
ENST00000696751.1:c.364+869G= ENSP00000512850.1:n.364+869G=
ENST00000231228.3:c.482+209G= MANE Select ENSP00000231228.2:n.482+209G=
ENST00000231228.2:c.482+209G= ENSP00000231228.2:n.482+209G=
NM_002187.2:c.482+209G= , LRG_71t1:c.482+209G= NP_002178.2:n.482+209G=
XR_001742945.1:n.147+1589C=
NM_002187.3:c.482+209G= MANE Select NP_002178.2:n.482+209G=
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