Canonical Allele Identifier: CA2776494896
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789317C>G , CM000669.2:g.74789317C>G GRCh38
NC_000007.13:g.74203661C>G , CM000669.1:g.74203661C>G GRCh37
NC_000007.12:g.73841597C>G NCBI36
NG_009078.2:g.20354C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.10:c.*157C>G ENSP00000289473.4:n.*157C>G
NM_000265.5:c.*157C>G NP_000256.4:n.*157C>G
XM_005250543.3:c.*251C>G XP_005250600.2:n.*251C>G
XM_011516498.1:c.*204C>G XP_011514800.1:n.*204C>G
XM_011516501.1:c.*157C>G XP_011514803.1:n.*157C>G
NM_000265.6:c.*157C>G NP_000256.4:n.*157C>G