Canonical Allele Identifier: CA1595018046
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322049T= , CM000667.2:g.159322049T= GRCh38
NC_000005.9:g.158749057T= , CM000667.1:g.158749057T= GRCh37
NC_000005.8:g.158681635T= NCBI36
NG_009618.1:g.13425A= , LRG_71:g.13425A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-1529A= ENSP00000512849.1:n.-148-1529A=
ENST00000696751.1:c.364+1005A= ENSP00000512850.1:n.364+1005A=
ENST00000231228.3:c.482+345A= MANE Select ENSP00000231228.2:n.482+345A=
ENST00000231228.2:c.482+345A= ENSP00000231228.2:n.482+345A=
NM_002187.2:c.482+345A= , LRG_71t1:c.482+345A= NP_002178.2:n.482+345A=
XR_001742945.1:n.147+1453T=
NM_002187.3:c.482+345A= MANE Select NP_002178.2:n.482+345A=
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