Canonical Allele Identifier: CA1595018345
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322781A= , CM000667.2:g.159322781A= GRCh38
NC_000005.9:g.158749789A= , CM000667.1:g.158749789A= GRCh37
NC_000005.8:g.158682367A= NCBI36
NG_009618.1:g.12693T= , LRG_71:g.12693T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2261T= ENSP00000512849.1:n.-148-2261T=
ENST00000696751.1:c.364+273T= ENSP00000512850.1:n.364+273T=
ENST00000231228.3:c.365-270T= MANE Select ENSP00000231228.2:n.365-270T=
ENST00000231228.2:c.365-270T= ENSP00000231228.2:n.365-270T=
NM_002187.2:c.365-270T= , LRG_71t1:c.365-270T= NP_002178.2:n.365-270T=
XR_001742945.1:n.147+2185A=
NM_002187.3:c.365-270T= MANE Select NP_002178.2:n.365-270T=
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