Canonical Allele Identifier: CA2676266283

Gene: IL12B

Linked Data

• gnomAD v4: 5-159322981-T-TTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322996_159322998dup , CM000667.2:g.159322996_159322998dup	GRCh38
NC_000005.9:g.158750004_158750006dup , CM000667.1:g.158750004_158750006dup	GRCh37
NC_000005.8:g.158682582_158682584dup	NCBI36
NG_009618.1:g.12490_12492dup , LRG_71:g.12490_12492dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2464_-148-2462dup	ENSP00000512849.1:n.-148-2464_-148-2462dup
ENST00000696751.1:c.364+70_364+72dup	ENSP00000512850.1:n.364+70_364+72dup
ENST00000231228.3:c.364+70_364+72dup MANE Select	ENSP00000231228.2:n.364+70_364+72dup
ENST00000231228.2:c.364+70_364+72dup	ENSP00000231228.2:n.364+70_364+72dup
NM_002187.2:c.364+70_364+72dup , LRG_71t1:c.364+70_364+72dup	NP_002178.2:n.364+70_364+72dup
XR_001742945.1:n.147+2400_147+2402dup
NM_002187.3:c.364+70_364+72dup MANE Select	NP_002178.2:n.364+70_364+72dup