Canonical Allele Identifier: CA1144128446

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183590710C= , CM000663.2:g.183590710C=	GRCh38
NC_000001.10:g.183559845C= , CM000663.1:g.183559845C=	GRCh37
NC_000001.9:g.181826468C=	NCBI36
NG_007267.1:g.4872G= , LRG_88:g.4872G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697330.1:c.-31+130G= (NCF2)	ENSP00000513258.1:n.-31+130G=
ENST00000367536.5:c.-31+130G= (NCF2)	ENSP00000356506.1:n.-31+130G=
ENST00000495321.1:n.234-7059C= (SMG7)
NM_001127651.2:c.-31+130G= (NCF2)	NP_001121123.1:n.-31+130G=
NM_001127651.3:c.-31+130G= (NCF2)	NP_001121123.1:n.-31+130G=