Canonical Allele Identifier: CA1717693204

Gene: NCF1

Linked Data

• dbSNP Id: rs1796734001

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789219C>T , CM000669.2:g.74789219C>T	GRCh38
NC_000007.13:g.74203563C>T , CM000669.1:g.74203563C>T	GRCh37
NC_000007.12:g.73841499C>T	NCBI36
NG_009078.2:g.20256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*59C>T MANE Select	ENSP00000289473.4:n.*59C>T
ENST00000289473.10:c.*59C>T	ENSP00000289473.4:n.*59C>T
ENST00000289473.8:c.*59C>T	ENSP00000289473.4:n.*59C>T
ENST00000398421.6:n.2259C>T
ENST00000455062.2:n.1341C>T
NM_000265.5:c.*59C>T	NP_000256.4:n.*59C>T
XM_005250543.3:c.*153C>T	XP_005250600.2:n.*153C>T
XM_011516498.1:c.*106C>T	XP_011514800.1:n.*106C>T
XM_011516501.1:c.*59C>T	XP_011514803.1:n.*59C>T
NM_000265.6:c.*59C>T	NP_000256.4:n.*59C>T
NM_000265.7:c.*59C>T MANE Select	NP_000256.4:n.*59C>T