Canonical Allele Identifier: CA1595018416
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322980A= , CM000667.2:g.159322980A= GRCh38
NC_000005.9:g.158749988A= , CM000667.1:g.158749988A= GRCh37
NC_000005.8:g.158682566A= NCBI36
NG_009618.1:g.12494T= , LRG_71:g.12494T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2460T= ENSP00000512849.1:n.-148-2460T=
ENST00000696751.1:c.364+74T= ENSP00000512850.1:n.364+74T=
ENST00000231228.3:c.364+74T= MANE Select ENSP00000231228.2:n.364+74T=
ENST00000231228.2:c.364+74T= ENSP00000231228.2:n.364+74T=
NM_002187.2:c.364+74T= , LRG_71t1:c.364+74T= NP_002178.2:n.364+74T=
XR_001742945.1:n.147+2384A=
NM_002187.3:c.364+74T= MANE Select NP_002178.2:n.364+74T=