Canonical Allele Identifier: CA1211968212

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183590702T= , CM000663.2:g.183590702T=	GRCh38
NC_000001.10:g.183559837T= , CM000663.1:g.183559837T=	GRCh37
NC_000001.9:g.181826460T=	NCBI36
NG_007267.1:g.4880A= , LRG_88:g.4880A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697330.1:c.-31+138A= (NCF2)	ENSP00000513258.1:n.-31+138A=
ENST00000697353.1:n.4A= (NCF2)
ENST00000367536.5:c.-31+138A= (NCF2)	ENSP00000356506.1:n.-31+138A=
ENST00000495321.1:n.234-7067T= (SMG7)
NM_001127651.2:c.-31+138A= (NCF2)	NP_001121123.1:n.-31+138A=
XM_011509580.1:c.-110A= (NCF2)	XP_011507882.1:n.-110A=
NM_001127651.3:c.-31+138A= (NCF2)	NP_001121123.1:n.-31+138A=