Canonical Allele Identifier: CA1211968206

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183590681C= , CM000663.2:g.183590681C=	GRCh38
NC_000001.10:g.183559816C= , CM000663.1:g.183559816C=	GRCh37
NC_000001.9:g.181826439C=	NCBI36
NG_007267.1:g.4901G= , LRG_88:g.4901G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697330.1:c.-31+159G= (NCF2)	ENSP00000513258.1:n.-31+159G=
ENST00000697353.1:n.25G= (NCF2)
ENST00000367536.5:c.-31+159G= (NCF2)	ENSP00000356506.1:n.-31+159G=
ENST00000495321.1:n.234-7088C= (SMG7)
NM_001127651.2:c.-31+159G= (NCF2)	NP_001121123.1:n.-31+159G=
XM_011509580.1:c.-89G= (NCF2)	XP_011507882.1:n.-89G=
NM_001127651.3:c.-31+159G= (NCF2)	NP_001121123.1:n.-31+159G=