Canonical Allele Identifier: CA362033000

Gene: IL12B

Linked Data

• dbSNP Id: rs565345523
• MyVariant Identifiers: chr5:g.158747505G>T (hg19) ; chr5:g.159320497G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320497G>T , CM000667.2:g.159320497G>T	GRCh38
NC_000005.9:g.158747505G>T , CM000667.1:g.158747505G>T	GRCh37
NC_000005.8:g.158680083G>T	NCBI36
NG_009618.1:g.14977C>A , LRG_71:g.14977C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-125C>A	ENSP00000512849.1:n.-125C>A
ENST00000696751.1:c.*1C>A	ENSP00000512850.1:n.*1C>A
ENST00000231228.3:c.506C>A MANE Select	ENSP00000231228.2:p.Thr169Lys
ENST00000231228.2:c.506C>A	ENSP00000231228.2:p.Thr169Lys
NM_002187.2:c.506C>A , LRG_71t1:c.506C>A	NP_002178.2:p.Thr169Lys
XR_001742945.1:n.48G>T
NM_002187.3:c.506C>A MANE Select	NP_002178.2:p.Thr169Lys