Canonical Allele Identifier: CA1717693281
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789353G= , CM000669.2:g.74789353G= GRCh38
NC_000007.13:g.74203697G= , CM000669.1:g.74203697G= GRCh37
NC_000007.12:g.73841633G= NCBI36
NG_009078.2:g.20390G=

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.10:c.*193G= ENSP00000289473.4:n.*193G=
NM_000265.5:c.*193G= NP_000256.4:n.*193G=
XM_005250543.3:c.*287G= XP_005250600.2:n.*287G=
XM_011516498.1:c.*240G= XP_011514800.1:n.*240G=
XM_011516501.1:c.*193G= XP_011514803.1:n.*193G=
NM_000265.6:c.*193G= NP_000256.4:n.*193G=