Canonical Allele Identifier: CA362032730

Gene: IL12B

Linked Data

• gnomAD v4: 5-159320414-T-C
• MyVariant Identifiers: chr5:g.158747422T>C (hg19) ; chr5:g.159320414T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320414T>C , CM000667.2:g.159320414T>C	GRCh38
NC_000005.9:g.158747422T>C , CM000667.1:g.158747422T>C	GRCh37
NC_000005.8:g.158680000T>C	NCBI36
NG_009618.1:g.15060A>G , LRG_71:g.15060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-42A>G	ENSP00000512849.1:n.-42A>G
ENST00000696751.1:c.*84A>G	ENSP00000512850.1:n.*84A>G
ENST00000231228.3:c.589A>G MANE Select	ENSP00000231228.2:p.Ser197Gly
ENST00000231228.2:c.589A>G	ENSP00000231228.2:p.Ser197Gly
NM_002187.2:c.589A>G , LRG_71t1:c.589A>G	NP_002178.2:p.Ser197Gly
NM_002187.3:c.589A>G MANE Select	NP_002178.2:p.Ser197Gly