Canonical Allele Identifier: CA362035342

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158750139A>T (hg19) ; chr5:g.159323131A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323131A>T , CM000667.2:g.159323131A>T	GRCh38
NC_000005.9:g.158750139A>T , CM000667.1:g.158750139A>T	GRCh37
NC_000005.8:g.158682717A>T	NCBI36
NG_009618.1:g.12343T>A , LRG_71:g.12343T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2611T>A	ENSP00000512849.1:n.-148-2611T>A
ENST00000696751.1:c.287T>A	ENSP00000512850.1:p.Val96Asp
ENST00000231228.3:c.287T>A MANE Select	ENSP00000231228.2:p.Val96Asp
ENST00000231228.2:c.287T>A	ENSP00000231228.2:p.Val96Asp
NM_002187.2:c.287T>A , LRG_71t1:c.287T>A	NP_002178.2:p.Val96Asp
XR_001742945.1:n.148-2403A>T
NM_002187.3:c.287T>A MANE Select	NP_002178.2:p.Val96Asp