Canonical Allele Identifier: CA1595018453
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323032C= , CM000667.2:g.159323032C= GRCh38
NC_000005.9:g.158750040C= , CM000667.1:g.158750040C= GRCh37
NC_000005.8:g.158682618C= NCBI36
NG_009618.1:g.12442G= , LRG_71:g.12442G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2512G= ENSP00000512849.1:n.-148-2512G=
ENST00000696751.1:c.364+22G= ENSP00000512850.1:n.364+22G=
ENST00000231228.3:c.364+22G= MANE Select ENSP00000231228.2:n.364+22G=
ENST00000231228.2:c.364+22G= ENSP00000231228.2:n.364+22G=
NM_002187.2:c.364+22G= , LRG_71t1:c.364+22G= NP_002178.2:n.364+22G=
XR_001742945.1:n.147+2436C=
NM_002187.3:c.364+22G= MANE Select NP_002178.2:n.364+22G=