Canonical Allele Identifier: CA362032511

Gene: IL12B

Linked Data

• gnomAD v3: 5-159320364-A-T
• gnomAD v4: 5-159320364-A-T
• MyVariant Identifiers: chr5:g.158747372A>T (hg19) ; chr5:g.159320364A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320364A>T , CM000667.2:g.159320364A>T	GRCh38
NC_000005.9:g.158747372A>T , CM000667.1:g.158747372A>T	GRCh37
NC_000005.8:g.158679950A>T	NCBI36
NG_009618.1:g.15110T>A , LRG_71:g.15110T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.9T>A	ENSP00000512849.1:p.Asp3Glu
ENST00000696751.1:c.*134T>A	ENSP00000512850.1:n.*134T>A
ENST00000231228.3:c.639T>A MANE Select	ENSP00000231228.2:p.Asp213Glu
ENST00000231228.2:c.639T>A	ENSP00000231228.2:p.Asp213Glu
NM_002187.2:c.639T>A , LRG_71t1:c.639T>A	NP_002178.2:p.Asp213Glu
NM_002187.3:c.639T>A MANE Select	NP_002178.2:p.Asp213Glu