Canonical Allele Identifier: CA2676266430

Gene: IL12B

Linked Data

• gnomAD v4: 5-159323091-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323092del , CM000667.2:g.159323092del	GRCh38
NC_000005.9:g.158750100del , CM000667.1:g.158750100del	GRCh37
NC_000005.8:g.158682678del	NCBI36
NG_009618.1:g.12382del , LRG_71:g.12382del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2572del	ENSP00000512849.1:n.-148-2572del
ENST00000696751.1:c.326del	ENSP00000512850.1:p.Asp109ValfsTer9
ENST00000231228.3:c.326del MANE Select	ENSP00000231228.2:p.Asp109ValfsTer9
ENST00000231228.2:c.326del	ENSP00000231228.2:p.Asp109ValfsTer9
NM_002187.2:c.326del , LRG_71t1:c.326del	NP_002178.2:p.Asp109ValfsTer9
XR_001742945.1:n.148-2442del
NM_002187.3:c.326del MANE Select	NP_002178.2:p.Asp109ValfsTer9