Canonical Allele Identifier: CA362032860

Gene: IL12B

Linked Data

• gnomAD v4: 5-159320442-A-C
• MyVariant Identifiers: chr5:g.158747450A>C (hg19) ; chr5:g.159320442A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320442A>C , CM000667.2:g.159320442A>C	GRCh38
NC_000005.9:g.158747450A>C , CM000667.1:g.158747450A>C	GRCh37
NC_000005.8:g.158680028A>C	NCBI36
NG_009618.1:g.15032T>G , LRG_71:g.15032T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-70T>G	ENSP00000512849.1:n.-70T>G
ENST00000696751.1:c.*56T>G	ENSP00000512850.1:n.*56T>G
ENST00000231228.3:c.561T>G MANE Select	ENSP00000231228.2:p.Tyr187Ter
ENST00000231228.2:c.561T>G	ENSP00000231228.2:p.Tyr187Ter
NM_002187.2:c.561T>G , LRG_71t1:c.561T>G	NP_002178.2:p.Tyr187Ter
NM_002187.3:c.561T>G MANE Select	NP_002178.2:p.Tyr187Ter