Canonical Allele Identifier: CA1717693221
Gene: NCF1 HGNC NCBI

Linked Data

dbSNP Id: rs1796734650
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789254G>A , CM000669.2:g.74789254G>A GRCh38
NC_000007.13:g.74203598G>A , CM000669.1:g.74203598G>A GRCh37
NC_000007.12:g.73841534G>A NCBI36
NG_009078.2:g.20291G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*94G>A MANE Select ENSP00000289473.4:n.*94G>A
ENST00000289473.10:c.*94G>A ENSP00000289473.4:n.*94G>A
ENST00000289473.8:c.*94G>A ENSP00000289473.4:n.*94G>A
ENST00000398421.6:n.2294G>A
ENST00000455062.2:n.1376G>A
NM_000265.5:c.*94G>A NP_000256.4:n.*94G>A
XM_005250543.3:c.*188G>A XP_005250600.2:n.*188G>A
XM_011516498.1:c.*141G>A XP_011514800.1:n.*141G>A
XM_011516501.1:c.*94G>A XP_011514803.1:n.*94G>A
NM_000265.6:c.*94G>A NP_000256.4:n.*94G>A
NM_000265.7:c.*94G>A MANE Select NP_000256.4:n.*94G>A
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