Canonical Allele Identifier: CA1595045725
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316074C= , CM000667.2:g.159316074C= GRCh38
NC_000005.9:g.158743082C= , CM000667.1:g.158743082C= GRCh37
NC_000005.8:g.158675660C= NCBI36
NG_009618.1:g.19400G= , LRG_71:g.19400G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*27G= ENSP00000512849.1:n.*27G=
ENST00000696751.1:c.*509G= ENSP00000512850.1:n.*509G=
ENST00000231228.3:c.*27G= MANE Select ENSP00000231228.2:n.*27G=
ENST00000231228.2:c.*27G= ENSP00000231228.2:n.*27G=
NM_002187.2:c.*27G= , LRG_71t1:c.*27G= NP_002178.2:n.*27G=
NM_002187.3:c.*27G= MANE Select NP_002178.2:n.*27G=