Canonical Allele Identifier: CA362035363

Gene: IL12B

Linked Data

• dbSNP Id: rs368468349
• MyVariant Identifiers: chr5:g.158750140C>T (hg19) ; chr5:g.159323132C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323132C>T , CM000667.2:g.159323132C>T	GRCh38
NC_000005.9:g.158750140C>T , CM000667.1:g.158750140C>T	GRCh37
NC_000005.8:g.158682718C>T	NCBI36
NG_009618.1:g.12342G>A , LRG_71:g.12342G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2612G>A	ENSP00000512849.1:n.-148-2612G>A
ENST00000696751.1:c.286G>A	ENSP00000512850.1:p.Val96Ile
ENST00000231228.3:c.286G>A MANE Select	ENSP00000231228.2:p.Val96Ile
ENST00000231228.2:c.286G>A	ENSP00000231228.2:p.Val96Ile
NM_002187.2:c.286G>A , LRG_71t1:c.286G>A	NP_002178.2:p.Val96Ile
XR_001742945.1:n.148-2402C>T
NM_002187.3:c.286G>A MANE Select	NP_002178.2:p.Val96Ile