Canonical Allele Identifier: CA1211968159

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183590585G= , CM000663.2:g.183590585G=	GRCh38
NC_000001.10:g.183559720G= , CM000663.1:g.183559720G=	GRCh37
NC_000001.9:g.181826343G=	NCBI36
NG_007267.1:g.4997C= , LRG_88:g.4997C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697330.1:c.-30-226C= (NCF2)	ENSP00000513258.1:n.-30-226C=
ENST00000697352.1:n.7C= (NCF2)
ENST00000697353.1:n.83+38C= (NCF2)
ENST00000367536.5:c.-30-226C= (NCF2)	ENSP00000356506.1:n.-30-226C=
ENST00000413720.5:c.-256C= (NCF2)	ENSP00000399294.1:n.-256C=
ENST00000418089.5:c.-256C= (NCF2)	ENSP00000407217.1:n.-256C=
ENST00000495321.1:n.234-7184G= (SMG7)
NM_000433.3:c.-256C= , LRG_88t1:c.-256C= (NCF2)	NP_000424.2:n.-256C=
NM_001127651.2:c.-30-226C= (NCF2)	NP_001121123.1:n.-30-226C=
NM_001190789.1:c.-256C= (NCF2)	NP_001177718.1:n.-256C=
NM_001190794.1:c.-256C= (NCF2)	NP_001177723.1:n.-256C=
XM_011509580.1:c.-31+38C= (NCF2)	XP_011507882.1:n.-31+38C=
XM_011509581.1:c.-94C= (NCF2)	XP_011507883.1:n.-94C=
NM_001127651.3:c.-30-226C= (NCF2)	NP_001121123.1:n.-30-226C=