Canonical Allele Identifier: CA1595018043
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322039A= , CM000667.2:g.159322039A= GRCh38
NC_000005.9:g.158749047A= , CM000667.1:g.158749047A= GRCh37
NC_000005.8:g.158681625A= NCBI36
NG_009618.1:g.13435T= , LRG_71:g.13435T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1519T= ENSP00000512849.1:n.-148-1519T=
ENST00000696751.1:c.364+1015T= ENSP00000512850.1:n.364+1015T=
ENST00000231228.3:c.482+355T= MANE Select ENSP00000231228.2:n.482+355T=
ENST00000231228.2:c.482+355T= ENSP00000231228.2:n.482+355T=
NM_002187.2:c.482+355T= , LRG_71t1:c.482+355T= NP_002178.2:n.482+355T=
XR_001742945.1:n.147+1443A=
NM_002187.3:c.482+355T= MANE Select NP_002178.2:n.482+355T=