Canonical Allele Identifier: CA362032302
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320326C>A , CM000667.2:g.159320326C>A GRCh38
NC_000005.9:g.158747334C>A , CM000667.1:g.158747334C>A GRCh37
NC_000005.8:g.158679912C>A NCBI36
NG_009618.1:g.15148G>T , LRG_71:g.15148G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.47G>T ENSP00000512849.1:p.Ser16Ile
ENST00000696751.1:c.*172G>T ENSP00000512850.1:n.*172G>T
ENST00000231228.3:c.677G>T MANE Select ENSP00000231228.2:p.Ser226Ile
ENST00000231228.2:c.677G>T ENSP00000231228.2:p.Ser226Ile
NM_002187.2:c.677G>T , LRG_71t1:c.677G>T NP_002178.2:p.Ser226Ile
NM_002187.3:c.677G>T MANE Select NP_002178.2:p.Ser226Ile