Canonical Allele Identifier: CA2683318114
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v4: 7-74789331-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789331A>G , CM000669.2:g.74789331A>G GRCh38
NC_000007.13:g.74203675A>G , CM000669.1:g.74203675A>G GRCh37
NC_000007.12:g.73841611A>G NCBI36
NG_009078.2:g.20368A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.10:c.*171A>G ENSP00000289473.4:n.*171A>G
NM_000265.5:c.*171A>G NP_000256.4:n.*171A>G
XM_005250543.3:c.*265A>G XP_005250600.2:n.*265A>G
XM_011516498.1:c.*218A>G XP_011514800.1:n.*218A>G
XM_011516501.1:c.*171A>G XP_011514803.1:n.*171A>G
NM_000265.6:c.*171A>G NP_000256.4:n.*171A>G