Canonical Allele Identifier: CA16044276
Gene: NCF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375467
ClinVar RCV Id: RCV000416494
dbSNP Id: rs1057519503

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789339G>A , CM000669.2:g.74789339G>A GRCh38
NC_000007.13:g.74203683G>A , CM000669.1:g.74203683G>A GRCh37
NC_000007.12:g.73841619G>A NCBI36
NG_009078.2:g.20376G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.10:c.*179G>A ENSP00000289473.4:n.*179G>A
NM_000265.5:c.*179G>A NP_000256.4:n.*179G>A
XM_005250543.3:c.*273G>A XP_005250600.2:n.*273G>A
XM_011516498.1:c.*226G>A XP_011514800.1:n.*226G>A
XM_011516501.1:c.*179G>A XP_011514803.1:n.*179G>A
NM_000265.6:c.*179G>A NP_000256.4:n.*179G>A