Canonical Allele Identifier: CA1717693291

Gene: NCF1

Linked Data

• dbSNP Id: rs1936026641

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789368C>T , CM000669.2:g.74789368C>T	GRCh38
NC_000007.13:g.74203712C>T , CM000669.1:g.74203712C>T	GRCh37
NC_000007.12:g.73841648C>T	NCBI36
NG_009078.2:g.20405C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.10:c.*208C>T	ENSP00000289473.4:n.*208C>T
NM_000265.5:c.*208C>T	NP_000256.4:n.*208C>T
XM_005250543.3:c.*302C>T	XP_005250600.2:n.*302C>T
XM_011516498.1:c.*255C>T	XP_011514800.1:n.*255C>T
XM_011516501.1:c.*208C>T	XP_011514803.1:n.*208C>T
NM_000265.6:c.*208C>T	NP_000256.4:n.*208C>T