Canonical Allele Identifier: CA362032854

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747448T>G (hg19) ; chr5:g.159320440T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320440T>G , CM000667.2:g.159320440T>G	GRCh38
NC_000005.9:g.158747448T>G , CM000667.1:g.158747448T>G	GRCh37
NC_000005.8:g.158680026T>G	NCBI36
NG_009618.1:g.15034A>C , LRG_71:g.15034A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-68A>C	ENSP00000512849.1:n.-68A>C
ENST00000696751.1:c.*58A>C	ENSP00000512850.1:n.*58A>C
ENST00000231228.3:c.563A>C MANE Select	ENSP00000231228.2:p.Glu188Ala
ENST00000231228.2:c.563A>C	ENSP00000231228.2:p.Glu188Ala
NM_002187.2:c.563A>C , LRG_71t1:c.563A>C	NP_002178.2:p.Glu188Ala
NM_002187.3:c.563A>C MANE Select	NP_002178.2:p.Glu188Ala