Canonical Allele Identifier: CA2683318121
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v4: 7-74789355-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789355C>T , CM000669.2:g.74789355C>T GRCh38
NC_000007.13:g.74203699C>T , CM000669.1:g.74203699C>T GRCh37
NC_000007.12:g.73841635C>T NCBI36
NG_009078.2:g.20392C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.10:c.*195C>T ENSP00000289473.4:n.*195C>T
NM_000265.5:c.*195C>T NP_000256.4:n.*195C>T
XM_005250543.3:c.*289C>T XP_005250600.2:n.*289C>T
XM_011516498.1:c.*242C>T XP_011514800.1:n.*242C>T
XM_011516501.1:c.*195C>T XP_011514803.1:n.*195C>T
NM_000265.6:c.*195C>T NP_000256.4:n.*195C>T