Canonical Allele Identifier: CA1717693269
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789339G= , CM000669.2:g.74789339G= GRCh38
NC_000007.13:g.74203683G= , CM000669.1:g.74203683G= GRCh37
NC_000007.12:g.73841619G= NCBI36
NG_009078.2:g.20376G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.10:c.*179G= ENSP00000289473.4:n.*179G=
NM_000265.5:c.*179G= NP_000256.4:n.*179G=
XM_005250543.3:c.*273G= XP_005250600.2:n.*273G=
XM_011516498.1:c.*226G= XP_011514800.1:n.*226G=
XM_011516501.1:c.*179G= XP_011514803.1:n.*179G=
NM_000265.6:c.*179G= NP_000256.4:n.*179G=