Canonical Allele Identifier: CA2600072478
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v3: 7-74789330-G-A
gnomAD v4: 7-74789330-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789330G>A , CM000669.2:g.74789330G>A GRCh38
NC_000007.13:g.74203674G>A , CM000669.1:g.74203674G>A GRCh37
NC_000007.12:g.73841610G>A NCBI36
NG_009078.2:g.20367G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.10:c.*170G>A ENSP00000289473.4:n.*170G>A
NM_000265.5:c.*170G>A NP_000256.4:n.*170G>A
XM_005250543.3:c.*264G>A XP_005250600.2:n.*264G>A
XM_011516498.1:c.*217G>A XP_011514800.1:n.*217G>A
XM_011516501.1:c.*170G>A XP_011514803.1:n.*170G>A
NM_000265.6:c.*170G>A NP_000256.4:n.*170G>A
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