Canonical Allele Identifier: CA1595017087
Gene: IL12B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159319961G= , CM000667.2:g.159319961G= GRCh38
NC_000005.9:g.158746969G= , CM000667.1:g.158746969G= GRCh37
NC_000005.8:g.158679547G= NCBI36
NG_009618.1:g.15513C= , LRG_71:g.15513C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+345C= ENSP00000512849.1:n.67+345C=
ENST00000696751.1:c.*192+345C= ENSP00000512850.1:n.*192+345C=
ENST00000231228.3:c.697+345C= MANE Select ENSP00000231228.2:n.697+345C=
ENST00000231228.2:c.697+345C= ENSP00000231228.2:n.697+345C=
NM_002187.2:c.697+345C= , LRG_71t1:c.697+345C= NP_002178.2:n.697+345C=
NM_002187.3:c.697+345C= MANE Select NP_002178.2:n.697+345C=
Search 100 bp 5'
Search 100 bp 3'