Canonical Allele Identifier: CA129826846

Gene: IL12B

Linked Data

• dbSNP Id: rs567462873
• gnomAD v4: 5-159320415-G-C
• MyVariant Identifiers: chr5:g.158747423G>C (hg19) ; chr5:g.159320415G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320415G>C , CM000667.2:g.159320415G>C	GRCh38
NC_000005.9:g.158747423G>C , CM000667.1:g.158747423G>C	GRCh37
NC_000005.8:g.158680001G>C	NCBI36
NG_009618.1:g.15059C>G , LRG_71:g.15059C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-43C>G	ENSP00000512849.1:n.-43C>G
ENST00000696751.1:c.*83C>G	ENSP00000512850.1:n.*83C>G
ENST00000231228.3:c.588C>G MANE Select	ENSP00000231228.2:p.Asp196Glu
ENST00000231228.2:c.588C>G	ENSP00000231228.2:p.Asp196Glu
NM_002187.2:c.588C>G , LRG_71t1:c.588C>G	NP_002178.2:p.Asp196Glu
NM_002187.3:c.588C>G MANE Select	NP_002178.2:p.Asp196Glu