Canonical Allele Identifier: CA1103162772

Gene: NCF1

Linked Data

• dbSNP Id: rs1796733210
• gnomAD v3: 7-74789179-A-G
• gnomAD v4: 7-74789179-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789179A>G , CM000669.2:g.74789179A>G	GRCh38
NC_000007.13:g.74203523A>G , CM000669.1:g.74203523A>G	GRCh37
NC_000007.12:g.73841459A>G	NCBI36
NG_009078.2:g.20216A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*19A>G MANE Select	ENSP00000289473.4:n.*19A>G
ENST00000289473.10:c.*19A>G	ENSP00000289473.4:n.*19A>G
ENST00000289473.8:c.*19A>G	ENSP00000289473.4:n.*19A>G
ENST00000398421.6:n.2219A>G
ENST00000455062.2:n.1301A>G
NM_000265.5:c.*19A>G	NP_000256.4:n.*19A>G
XM_005250543.3:c.*113A>G	XP_005250600.2:n.*113A>G
XM_011516498.1:c.*66A>G	XP_011514800.1:n.*66A>G
XM_011516501.1:c.*19A>G	XP_011514803.1:n.*19A>G
NM_000265.6:c.*19A>G	NP_000256.4:n.*19A>G
NM_000265.7:c.*19A>G MANE Select	NP_000256.4:n.*19A>G