Canonical Allele Identifier: CA447510741

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747321C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320313C>T , CM000667.2:g.159320313C>T	GRCh38
NC_000005.9:g.158747321C>T , CM000667.1:g.158747321C>T	GRCh37
NC_000005.8:g.158679899C>T	NCBI36
NG_009618.1:g.15161G>A , LRG_71:g.15161G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.60G>A	ENSP00000512849.1:p.Arg20=
ENST00000696751.1:c.*185G>A	ENSP00000512850.1:n.*185G>A
ENST00000231228.3:c.690G>A MANE Select	ENSP00000231228.2:p.Arg230=
ENST00000231228.2:c.690G>A	ENSP00000231228.2:p.Arg230=
NM_002187.2:c.690G>A , LRG_71t1:c.690G>A	NP_002178.2:p.Arg230=
NM_002187.3:c.690G>A MANE Select	NP_002178.2:p.Arg230=