Canonical Allele Identifier: CA1595045186

Gene: IL12B

Linked Data

• dbSNP Id: rs1753963454
• gnomAD v4: 5-159314908-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159314908C>A , CM000667.2:g.159314908C>A	GRCh38
NC_000005.9:g.158741916C>A , CM000667.1:g.158741916C>A	GRCh37
NC_000005.8:g.158674494C>A	NCBI36
NG_009618.1:g.20566G>T , LRG_71:g.20566G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1193G>T	ENSP00000512849.1:n.*1193G>T
ENST00000696751.1:c.*1675G>T	ENSP00000512850.1:n.*1675G>T
ENST00000231228.3:c.*1193G>T MANE Select	ENSP00000231228.2:n.*1193G>T
ENST00000231228.2:c.*1193G>T	ENSP00000231228.2:n.*1193G>T
NM_002187.2:c.*1193G>T , LRG_71t1:c.*1193G>T	NP_002178.2:n.*1193G>T
XR_941138.1:n.364-310C>A
XR_941138.2:n.431-310C>A
NM_002187.3:c.*1193G>T MANE Select	NP_002178.2:n.*1193G>T