Canonical Allele Identifier: CA1595018015

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321988_159321991delinsCAGG , CM000667.2:g.159321988_159321991delinsCAGG	GRCh38
NC_000005.9:g.158748996_158748999delinsCAGG , CM000667.1:g.158748996_158748999delinsCAGG	GRCh37
NC_000005.8:g.158681574_158681577delinsCAGG	NCBI36
NG_009618.1:g.13483_13486delinsCCTG , LRG_71:g.13483_13486delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1471_-148-1468delinsCCTG	ENSP00000512849.1:n.-148-1471_-148-1468delinsCCTG
ENST00000696751.1:c.364+1063_364+1066delinsCCTG	ENSP00000512850.1:n.364+1063_364+1066delinsCCTG
ENST00000231228.3:c.482+403_482+406delinsCCTG MANE Select	ENSP00000231228.2:n.482+403_482+406delinsCCTG
ENST00000231228.2:c.482+403_482+406delinsCCTG	ENSP00000231228.2:n.482+403_482+406delinsCCTG
NM_002187.2:c.482+403_482+406delinsCCTG , LRG_71t1:c.482+403_482+406delinsCCTG	NP_002178.2:n.482+403_482+406delinsCCTG
XR_001742945.1:n.147+1392_147+1395delinsCAGG
NM_002187.3:c.482+403_482+406delinsCCTG MANE Select	NP_002178.2:n.482+403_482+406delinsCCTG