Canonical Allele Identifier: CA1103162935
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v3: 7-74789335-C-T
gnomAD v4: 7-74789335-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789335C>T , CM000669.2:g.74789335C>T GRCh38
NC_000007.13:g.74203679C>T , CM000669.1:g.74203679C>T GRCh37
NC_000007.12:g.73841615C>T NCBI36
NG_009078.2:g.20372C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.10:c.*175C>T ENSP00000289473.4:n.*175C>T
NM_000265.5:c.*175C>T NP_000256.4:n.*175C>T
XM_005250543.3:c.*269C>T XP_005250600.2:n.*269C>T
XM_011516498.1:c.*222C>T XP_011514800.1:n.*222C>T
XM_011516501.1:c.*175C>T XP_011514803.1:n.*175C>T
NM_000265.6:c.*175C>T NP_000256.4:n.*175C>T
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