Canonical Allele Identifier: CA575374898

Gene: NCF1

Linked Data

• dbSNP Id: rs1554414113
• gnomAD v2: 7-74197847-A-G
• gnomAD v4: 7-74783504-A-G
• MyVariant Identifiers: chr7:g.74197847A>G (hg19) ; chr7:g.74783504A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783504A>G , CM000669.2:g.74783504A>G	GRCh38
NC_000007.13:g.74197847A>G , CM000669.1:g.74197847A>G	GRCh37
NC_000007.12:g.73835783A>G	NCBI36
NG_009078.2:g.14541A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.575-21A>G MANE Select	ENSP00000289473.4:n.575-21A>G
ENST00000289473.10:c.575-21A>G	ENSP00000289473.4:n.575-21A>G
ENST00000289473.8:c.575-21A>G	ENSP00000289473.4:n.575-21A>G
ENST00000398421.6:n.1111A>G
ENST00000443956.7:n.696-21A>G
ENST00000449343.6:n.1038A>G
ENST00000455062.2:n.701A>G
ENST00000464878.5:c.867A>G
ENST00000486097.1:n.62A>G
NM_000265.5:c.575-21A>G	NP_000256.4:n.575-21A>G
XM_005250543.3:c.575-21A>G	XP_005250600.2:n.575-21A>G
XM_005250544.3:c.575-21A>G	XP_005250601.2:n.575-21A>G
XM_011516498.1:c.575-21A>G	XP_011514800.1:n.575-21A>G
XM_011516499.1:c.575-21A>G	XP_011514801.1:n.575-21A>G
XM_011516500.1:c.575-21A>G	XP_011514802.1:n.575-21A>G
XM_011516501.1:c.182-21A>G	XP_011514803.1:n.182-21A>G
XR_242262.3:n.630-21A>G
XR_927515.1:n.630-21A>G
NM_000265.6:c.575-21A>G	NP_000256.4:n.575-21A>G
NM_000265.7:c.575-21A>G MANE Select	NP_000256.4:n.575-21A>G