Canonical Allele Identifier: CA2676265677

Gene: IL12B

Linked Data

• gnomAD v4: 5-159322262-C-CCGATT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322262_159322263insCGATT , CM000667.2:g.159322262_159322263insCGATT	GRCh38
NC_000005.9:g.158749270_158749271insCGATT , CM000667.1:g.158749270_158749271insCGATT	GRCh37
NC_000005.8:g.158681848_158681849insCGATT	NCBI36
NG_009618.1:g.13211_13212insAATCG , LRG_71:g.13211_13212insAATCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1743_-148-1742insAATCG	ENSP00000512849.1:n.-148-1743_-148-1742insAATCG
ENST00000696751.1:c.364+791_364+792insAATCG	ENSP00000512850.1:n.364+791_364+792insAATCG
ENST00000231228.3:c.482+131_482+132insAATCG MANE Select	ENSP00000231228.2:n.482+131_482+132insAATCG
ENST00000231228.2:c.482+131_482+132insAATCG	ENSP00000231228.2:n.482+131_482+132insAATCG
NM_002187.2:c.482+131_482+132insAATCG , LRG_71t1:c.482+131_482+132insAATCG	NP_002178.2:n.482+131_482+132insAATCG
XR_001742945.1:n.147+1666_147+1667insCGATT
NM_002187.3:c.482+131_482+132insAATCG MANE Select	NP_002178.2:n.482+131_482+132insAATCG