Canonical Allele Identifier: CA842143327

Gene: NCF1

Linked Data

• dbSNP Id: rs1257951785
• MyVariant Identifiers: chr7:g.74789282C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789282C>T , CM000669.2:g.74789282C>T	GRCh38
NC_000007.13:g.74203626C>T , CM000669.1:g.74203626C>T	GRCh37
NC_000007.12:g.73841562C>T	NCBI36
NG_009078.2:g.20319C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*122C>T MANE Select	ENSP00000289473.4:n.*122C>T
ENST00000289473.10:c.*122C>T	ENSP00000289473.4:n.*122C>T
ENST00000289473.8:c.*122C>T	ENSP00000289473.4:n.*122C>T
ENST00000398421.6:n.2322C>T
ENST00000455062.2:n.1404C>T
NM_000265.5:c.*122C>T	NP_000256.4:n.*122C>T
XM_005250543.3:c.*216C>T	XP_005250600.2:n.*216C>T
XM_011516498.1:c.*169C>T	XP_011514800.1:n.*169C>T
XM_011516501.1:c.*122C>T	XP_011514803.1:n.*122C>T
NM_000265.6:c.*122C>T	NP_000256.4:n.*122C>T
NM_000265.7:c.*122C>T MANE Select	NP_000256.4:n.*122C>T