Canonical Allele Identifier: CA2683318113

Gene: NCF1

Linked Data

• gnomAD v4: 7-74789328-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789328A>G , CM000669.2:g.74789328A>G	GRCh38
NC_000007.13:g.74203672A>G , CM000669.1:g.74203672A>G	GRCh37
NC_000007.12:g.73841608A>G	NCBI36
NG_009078.2:g.20365A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.10:c.*168A>G	ENSP00000289473.4:n.*168A>G
NM_000265.5:c.*168A>G	NP_000256.4:n.*168A>G
XM_005250543.3:c.*262A>G	XP_005250600.2:n.*262A>G
XM_011516498.1:c.*215A>G	XP_011514800.1:n.*215A>G
XM_011516501.1:c.*168A>G	XP_011514803.1:n.*168A>G
NM_000265.6:c.*168A>G	NP_000256.4:n.*168A>G