Canonical Allele Identifier: CA1595045717
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316044A= , CM000667.2:g.159316044A= GRCh38
NC_000005.9:g.158743052A= , CM000667.1:g.158743052A= GRCh37
NC_000005.8:g.158675630A= NCBI36
NG_009618.1:g.19430T= , LRG_71:g.19430T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*57T= ENSP00000512849.1:n.*57T=
ENST00000696751.1:c.*539T= ENSP00000512850.1:n.*539T=
ENST00000231228.3:c.*57T= MANE Select ENSP00000231228.2:n.*57T=
ENST00000231228.2:c.*57T= ENSP00000231228.2:n.*57T=
NM_002187.2:c.*57T= , LRG_71t1:c.*57T= NP_002178.2:n.*57T=
NM_002187.3:c.*57T= MANE Select NP_002178.2:n.*57T=