Canonical Allele Identifier: CA367955769

Gene: NCF1

Linked Data

• dbSNP Id: rs1796730381
• MyVariant Identifiers: chr7:g.74203383A>G (hg19) ; chr7:g.74789039A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789039A>G , CM000669.2:g.74789039A>G	GRCh38
NC_000007.13:g.74203383A>G , CM000669.1:g.74203383A>G	GRCh37
NC_000007.12:g.73841319A>G	NCBI36
NG_009078.2:g.20076A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052A>G MANE Select	ENSP00000289473.4:p.Glu351Gly
ENST00000289473.10:c.1052A>G	ENSP00000289473.4:p.Glu351Gly
ENST00000289473.8:c.1052A>G	ENSP00000289473.4:p.Glu351Gly
ENST00000398421.6:n.2079A>G
ENST00000455062.2:n.1161A>G
NM_000265.5:c.1052A>G	NP_000256.4:p.Glu351Gly
XM_005250543.3:c.1014A>G	XP_005250600.2:p.Arg338=
XM_011516498.1:c.1051A>G	XP_011514800.1:p.Arg351Gly
XM_011516501.1:c.659A>G	XP_011514803.1:p.Glu220Gly
NM_000265.6:c.1052A>G	NP_000256.4:p.Glu351Gly
NM_000265.7:c.1052A>G MANE Select	NP_000256.4:p.Glu351Gly