Canonical Allele Identifier: CA2776494898
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789360G>T , CM000669.2:g.74789360G>T GRCh38
NC_000007.13:g.74203704G>T , CM000669.1:g.74203704G>T GRCh37
NC_000007.12:g.73841640G>T NCBI36
NG_009078.2:g.20397G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.10:c.*200G>T ENSP00000289473.4:n.*200G>T
NM_000265.5:c.*200G>T NP_000256.4:n.*200G>T
XM_005250543.3:c.*294G>T XP_005250600.2:n.*294G>T
XM_011516498.1:c.*247G>T XP_011514800.1:n.*247G>T
XM_011516501.1:c.*200G>T XP_011514803.1:n.*200G>T
NM_000265.6:c.*200G>T NP_000256.4:n.*200G>T