Canonical Allele Identifier: CA1103162932

Gene: NCF1

Linked Data

• dbSNP Id: rs1796735918
• gnomAD v3: 7-74789315-AC-A
• gnomAD v4: 7-74789315-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789317del , CM000669.2:g.74789317del	GRCh38
NC_000007.13:g.74203661del , CM000669.1:g.74203661del	GRCh37
NC_000007.12:g.73841597del	NCBI36
NG_009078.2:g.20354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.10:c.*157del	ENSP00000289473.4:n.*157del
NM_000265.5:c.*157del	NP_000256.4:n.*157del
XM_005250543.3:c.*251del	XP_005250600.2:n.*251del
XM_011516498.1:c.*204del	XP_011514800.1:n.*204del
XM_011516501.1:c.*157del	XP_011514803.1:n.*157del
NM_000265.6:c.*157del	NP_000256.4:n.*157del