Canonical Allele Identifier: CA129823286

Gene: IL12B

Linked Data

• dbSNP Id: rs1032250693
• MyVariant Identifiers: chr5:g.158743052A>T (hg19) ; chr5:g.159316044A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316044A>T , CM000667.2:g.159316044A>T	GRCh38
NC_000005.9:g.158743052A>T , CM000667.1:g.158743052A>T	GRCh37
NC_000005.8:g.158675630A>T	NCBI36
NG_009618.1:g.19430T>A , LRG_71:g.19430T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*57T>A	ENSP00000512849.1:n.*57T>A
ENST00000696751.1:c.*539T>A	ENSP00000512850.1:n.*539T>A
ENST00000231228.3:c.*57T>A MANE Select	ENSP00000231228.2:n.*57T>A
ENST00000231228.2:c.*57T>A	ENSP00000231228.2:n.*57T>A
NM_002187.2:c.*57T>A , LRG_71t1:c.*57T>A	NP_002178.2:n.*57T>A
NM_002187.3:c.*57T>A MANE Select	NP_002178.2:n.*57T>A