Canonical Allele Identifier: CA362032837

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747445T>C (hg19) ; chr5:g.159320437T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320437T>C , CM000667.2:g.159320437T>C	GRCh38
NC_000005.9:g.158747445T>C , CM000667.1:g.158747445T>C	GRCh37
NC_000005.8:g.158680023T>C	NCBI36
NG_009618.1:g.15037A>G , LRG_71:g.15037A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-65A>G	ENSP00000512849.1:n.-65A>G
ENST00000696751.1:c.*61A>G	ENSP00000512850.1:n.*61A>G
ENST00000231228.3:c.566A>G MANE Select	ENSP00000231228.2:p.Tyr189Cys
ENST00000231228.2:c.566A>G	ENSP00000231228.2:p.Tyr189Cys
NM_002187.2:c.566A>G , LRG_71t1:c.566A>G	NP_002178.2:p.Tyr189Cys
NM_002187.3:c.566A>G MANE Select	NP_002178.2:p.Tyr189Cys