Canonical Allele Identifier: CA1595045669
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315941C= , CM000667.2:g.159315941C= GRCh38
NC_000005.9:g.158742949C= , CM000667.1:g.158742949C= GRCh37
NC_000005.8:g.158675527C= NCBI36
NG_009618.1:g.19533G= , LRG_71:g.19533G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*160G= ENSP00000512849.1:n.*160G=
ENST00000696751.1:c.*642G= ENSP00000512850.1:n.*642G=
ENST00000231228.3:c.*160G= MANE Select ENSP00000231228.2:n.*160G=
ENST00000231228.2:c.*160G= ENSP00000231228.2:n.*160G=
NM_002187.2:c.*160G= , LRG_71t1:c.*160G= NP_002178.2:n.*160G=
NM_002187.3:c.*160G= MANE Select NP_002178.2:n.*160G=