Canonical Allele Identifier: CA2683318123
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v4: 7-74789374-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789374T>G , CM000669.2:g.74789374T>G GRCh38
NC_000007.13:g.74203718T>G , CM000669.1:g.74203718T>G GRCh37
NC_000007.12:g.73841654T>G NCBI36
NG_009078.2:g.20411T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.10:c.*214T>G ENSP00000289473.4:n.*214T>G
NM_000265.5:c.*214T>G NP_000256.4:n.*214T>G
XM_005250543.3:c.*308T>G XP_005250600.2:n.*308T>G
XM_011516498.1:c.*261T>G XP_011514800.1:n.*261T>G
XM_011516501.1:c.*214T>G XP_011514803.1:n.*214T>G
NM_000265.6:c.*214T>G NP_000256.4:n.*214T>G