Canonical Allele Identifier: CA362036418
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323230T>A , CM000667.2:g.159323230T>A GRCh38
NC_000005.9:g.158750238T>A , CM000667.1:g.158750238T>A GRCh37
NC_000005.8:g.158682816T>A NCBI36
NG_009618.1:g.12244A>T , LRG_71:g.12244A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2710A>T ENSP00000512849.1:n.-148-2710A>T
ENST00000696751.1:c.188A>T ENSP00000512850.1:p.Asp63Val
ENST00000231228.3:c.188A>T MANE Select ENSP00000231228.2:p.Asp63Val
ENST00000231228.2:c.188A>T ENSP00000231228.2:p.Asp63Val
NM_002187.2:c.188A>T , LRG_71t1:c.188A>T NP_002178.2:p.Asp63Val
XR_001742945.1:n.148-2304T>A
NM_002187.3:c.188A>T MANE Select NP_002178.2:p.Asp63Val