Canonical Allele Identifier: CA1103162937

Gene: NCF1

Linked Data

• dbSNP Id: rs1796736149
• gnomAD v3: 7-74789343-G-T
• gnomAD v4: 7-74789343-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789343G>T , CM000669.2:g.74789343G>T	GRCh38
NC_000007.13:g.74203687G>T , CM000669.1:g.74203687G>T	GRCh37
NC_000007.12:g.73841623G>T	NCBI36
NG_009078.2:g.20380G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.10:c.*183G>T	ENSP00000289473.4:n.*183G>T
NM_000265.5:c.*183G>T	NP_000256.4:n.*183G>T
XM_005250543.3:c.*277G>T	XP_005250600.2:n.*277G>T
XM_011516498.1:c.*230G>T	XP_011514800.1:n.*230G>T
XM_011516501.1:c.*183G>T	XP_011514803.1:n.*183G>T
NM_000265.6:c.*183G>T	NP_000256.4:n.*183G>T