Canonical Allele Identifier: CA1717693280

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789344C= , CM000669.2:g.74789344C=	GRCh38
NC_000007.13:g.74203688C= , CM000669.1:g.74203688C=	GRCh37
NC_000007.12:g.73841624C=	NCBI36
NG_009078.2:g.20381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.10:c.*184C=	ENSP00000289473.4:n.*184C=
NM_000265.5:c.*184C=	NP_000256.4:n.*184C=
XM_005250543.3:c.*278C=	XP_005250600.2:n.*278C=
XM_011516498.1:c.*231C=	XP_011514800.1:n.*231C=
XM_011516501.1:c.*184C=	XP_011514803.1:n.*184C=
NM_000265.6:c.*184C=	NP_000256.4:n.*184C=