Canonical Allele Identifier: CA2715262235
Gene: NCF1 HGNC NCBI

Linked Data

dbSNP Id: rs2131610283

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789241C>G , CM000669.2:g.74789241C>G GRCh38
NC_000007.13:g.74203585C>G , CM000669.1:g.74203585C>G GRCh37
NC_000007.12:g.73841521C>G NCBI36
NG_009078.2:g.20278C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*81C>G MANE Select ENSP00000289473.4:n.*81C>G
ENST00000289473.10:c.*81C>G ENSP00000289473.4:n.*81C>G
ENST00000289473.8:c.*81C>G ENSP00000289473.4:n.*81C>G
ENST00000398421.6:n.2281C>G
ENST00000455062.2:n.1363C>G
NM_000265.5:c.*81C>G NP_000256.4:n.*81C>G
XM_005250543.3:c.*175C>G XP_005250600.2:n.*175C>G
XM_011516498.1:c.*128C>G XP_011514800.1:n.*128C>G
XM_011516501.1:c.*81C>G XP_011514803.1:n.*81C>G
NM_000265.6:c.*81C>G NP_000256.4:n.*81C>G
NM_000265.7:c.*81C>G MANE Select NP_000256.4:n.*81C>G