Canonical Allele Identifier: CA2649486398

Gene: NCF2 SMG7

Linked Data

• gnomAD v4: 1-183590736-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183590736A>T , CM000663.2:g.183590736A>T	GRCh38
NC_000001.10:g.183559871A>T , CM000663.1:g.183559871A>T	GRCh37
NC_000001.9:g.181826494A>T	NCBI36
NG_007267.1:g.4846T>A , LRG_88:g.4846T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697330.1:c.-31+104T>A (NCF2)	ENSP00000513258.1:n.-31+104T>A
ENST00000367536.5:c.-31+104T>A (NCF2)	ENSP00000356506.1:n.-31+104T>A
ENST00000495321.1:n.234-7033A>T (SMG7)
NM_001127651.2:c.-31+104T>A (NCF2)	NP_001121123.1:n.-31+104T>A
NM_001127651.3:c.-31+104T>A (NCF2)	NP_001121123.1:n.-31+104T>A