Canonical Allele Identifier: CA1595045693
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315988G= , CM000667.2:g.159315988G= GRCh38
NC_000005.9:g.158742996G= , CM000667.1:g.158742996G= GRCh37
NC_000005.8:g.158675574G= NCBI36
NG_009618.1:g.19486C= , LRG_71:g.19486C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*113C= ENSP00000512849.1:n.*113C=
ENST00000696751.1:c.*595C= ENSP00000512850.1:n.*595C=
ENST00000231228.3:c.*113C= MANE Select ENSP00000231228.2:n.*113C=
ENST00000231228.2:c.*113C= ENSP00000231228.2:n.*113C=
NM_002187.2:c.*113C= , LRG_71t1:c.*113C= NP_002178.2:n.*113C=
NM_002187.3:c.*113C= MANE Select NP_002178.2:n.*113C=