Canonical Allele Identifier: CA362032166

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747314T>A (hg19) ; chr5:g.159320306T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320306T>A , CM000667.2:g.159320306T>A	GRCh38
NC_000005.9:g.158747314T>A , CM000667.1:g.158747314T>A	GRCh37
NC_000005.8:g.158679892T>A	NCBI36
NG_009618.1:g.15168A>T , LRG_71:g.15168A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67A>T	ENSP00000512849.1:p.Ile23Phe
ENST00000696751.1:c.*192A>T	ENSP00000512850.1:n.*192A>T
ENST00000231228.3:c.697A>T MANE Select	ENSP00000231228.2:p.Ile233Phe
ENST00000231228.2:c.697A>T	ENSP00000231228.2:p.Ile233Phe
NM_002187.2:c.697A>T , LRG_71t1:c.697A>T	NP_002178.2:p.Ile233Phe
NM_002187.3:c.697A>T MANE Select	NP_002178.2:p.Ile233Phe