Canonical Allele Identifier: CA129826486

Gene: IL12B

Linked Data

• dbSNP Id: rs530045589
• MyVariant Identifiers: chr5:g.158747043T>A (hg19) ; chr5:g.159320035T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320035T>A , CM000667.2:g.159320035T>A	GRCh38
NC_000005.9:g.158747043T>A , CM000667.1:g.158747043T>A	GRCh37
NC_000005.8:g.158679621T>A	NCBI36
NG_009618.1:g.15439A>T , LRG_71:g.15439A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+271A>T	ENSP00000512849.1:n.67+271A>T
ENST00000696751.1:c.*192+271A>T	ENSP00000512850.1:n.*192+271A>T
ENST00000231228.3:c.697+271A>T MANE Select	ENSP00000231228.2:n.697+271A>T
ENST00000231228.2:c.697+271A>T	ENSP00000231228.2:n.697+271A>T
NM_002187.2:c.697+271A>T , LRG_71t1:c.697+271A>T	NP_002178.2:n.697+271A>T
NM_002187.3:c.697+271A>T MANE Select	NP_002178.2:n.697+271A>T