Canonical Allele Identifier: CA1595018132

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322272_159322274delinsAAC , CM000667.2:g.159322272_159322274delinsAAC	GRCh38
NC_000005.9:g.158749280_158749282delinsAAC , CM000667.1:g.158749280_158749282delinsAAC	GRCh37
NC_000005.8:g.158681858_158681860delinsAAC	NCBI36
NG_009618.1:g.13200_13202delinsGTT , LRG_71:g.13200_13202delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1754_-148-1752delinsGTT	ENSP00000512849.1:n.-148-1754_-148-1752delinsGTT
ENST00000696751.1:c.364+780_364+782delinsGTT	ENSP00000512850.1:n.364+780_364+782delinsGTT
ENST00000231228.3:c.482+120_482+122delinsGTT MANE Select	ENSP00000231228.2:n.482+120_482+122delinsGTT
ENST00000231228.2:c.482+120_482+122delinsGTT	ENSP00000231228.2:n.482+120_482+122delinsGTT
NM_002187.2:c.482+120_482+122delinsGTT , LRG_71t1:c.482+120_482+122delinsGTT	NP_002178.2:n.482+120_482+122delinsGTT
XR_001742945.1:n.147+1676_147+1678delinsAAC
NM_002187.3:c.482+120_482+122delinsGTT MANE Select	NP_002178.2:n.482+120_482+122delinsGTT