Canonical Allele Identifier: CA129822655

Gene: IL12B

Linked Data

• dbSNP Id: rs994513840
• gnomAD v3: 5-159315044-T-C
• gnomAD v4: 5-159315044-T-C
• MyVariant Identifiers: chr5:g.158742052T>C (hg19) ; chr5:g.159315044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315044T>C , CM000667.2:g.159315044T>C	GRCh38
NC_000005.9:g.158742052T>C , CM000667.1:g.158742052T>C	GRCh37
NC_000005.8:g.158674630T>C	NCBI36
NG_009618.1:g.20430A>G , LRG_71:g.20430A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1057A>G	ENSP00000512849.1:n.*1057A>G
ENST00000696751.1:c.*1539A>G	ENSP00000512850.1:n.*1539A>G
ENST00000231228.3:c.*1057A>G MANE Select	ENSP00000231228.2:n.*1057A>G
ENST00000231228.2:c.*1057A>G	ENSP00000231228.2:n.*1057A>G
NM_002187.2:c.*1057A>G , LRG_71t1:c.*1057A>G	NP_002178.2:n.*1057A>G
XR_941138.1:n.364-174T>C
XR_941138.2:n.431-174T>C
NM_002187.3:c.*1057A>G MANE Select	NP_002178.2:n.*1057A>G