Canonical Allele Identifier: CA129823187

Gene: IL12B

Linked Data

• dbSNP Id: rs748031214
• MyVariant Identifiers: chr5:g.158742949C>T (hg19) ; chr5:g.159315941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315941C>T , CM000667.2:g.159315941C>T	GRCh38
NC_000005.9:g.158742949C>T , CM000667.1:g.158742949C>T	GRCh37
NC_000005.8:g.158675527C>T	NCBI36
NG_009618.1:g.19533G>A , LRG_71:g.19533G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.*160G>A	ENSP00000512849.1:n.*160G>A
ENST00000696751.1:c.*642G>A	ENSP00000512850.1:n.*642G>A
ENST00000231228.3:c.*160G>A MANE Select	ENSP00000231228.2:n.*160G>A
ENST00000231228.2:c.*160G>A	ENSP00000231228.2:n.*160G>A
NM_002187.2:c.*160G>A , LRG_71t1:c.*160G>A	NP_002178.2:n.*160G>A
NM_002187.3:c.*160G>A MANE Select	NP_002178.2:n.*160G>A