Canonical Allele Identifier: CA362033033

Gene: IL12B

Linked Data

• gnomAD v4: 5-159320513-C-A
• MyVariant Identifiers: chr5:g.158747521C>A (hg19) ; chr5:g.159320513C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320513C>A , CM000667.2:g.159320513C>A	GRCh38
NC_000005.9:g.158747521C>A , CM000667.1:g.158747521C>A	GRCh37
NC_000005.8:g.158680099C>A	NCBI36
NG_009618.1:g.14961G>T , LRG_71:g.14961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-141G>T	ENSP00000512849.1:n.-141G>T
ENST00000696751.1:c.372G>T	ENSP00000512850.1:p.Leu124=
ENST00000231228.3:c.490G>T MANE Select	ENSP00000231228.2:p.Asp164Tyr
ENST00000231228.2:c.490G>T	ENSP00000231228.2:p.Asp164Tyr
NM_002187.2:c.490G>T , LRG_71t1:c.490G>T	NP_002178.2:p.Asp164Tyr
XR_001742945.1:n.64C>A
NM_002187.3:c.490G>T MANE Select	NP_002178.2:p.Asp164Tyr