Canonical Allele Identifier: CA10212870

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs369350039
• ExAC: 22:37260966 C / T
• gnomAD v2: 22-37260966-C-T
• gnomAD v3: 22-36864924-C-T
• gnomAD v4: 22-36864924-C-T
• MyVariant Identifiers: chr22:g.37260966C>T (hg19) ; chr22:g.36864924C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864924C>T , CM000684.2:g.36864924C>T	GRCh38
NC_000022.10:g.37260966C>T , CM000684.1:g.37260966C>T	GRCh37
NC_000022.9:g.35590912C>T	NCBI36
NG_023400.1:g.8937C>T , LRG_159:g.8937C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.123C>T (NCF4) MANE Select	ENSP00000248899.6:p.Phe41=
ENST00000397147.7:c.123C>T (NCF4)	ENSP00000380334.4:p.Phe41=
ENST00000650698.1:c.-187C>T (NCF4)	ENSP00000498381.1:n.-187C>T
ENST00000650827.1:c.-187C>T (NCF4)	ENSP00000498212.1:n.-187C>T
ENST00000651053.1:n.428C>T (NCF4)
ENST00000248899.10:c.123C>T (NCF4)	ENSP00000248899.6:p.Phe41=
ENST00000397147.6:c.123C>T (NCF4)	ENSP00000380334.4:p.Phe41=
ENST00000447071.5:c.-187C>T (NCF4)	ENSP00000414958.1:n.-187C>T
NM_000631.4:c.123C>T (NCF4)	NP_000622.2:p.Phe41=
NM_013416.3:c.123C>T , LRG_159t1:c.123C>T (NCF4)	NP_038202.2:p.Phe41=
XM_011530198.1:c.297C>T (NCF4)	XP_011528500.1:p.Phe99=
XM_011530199.1:c.267C>T (NCF4)	XP_011528501.1:p.Phe89=
NR_147197.1:n.351+5169G>A (NCF4-AS1)
XM_017028808.1:c.-187C>T (NCF4)	XP_016884297.1:n.-187C>T
NM_000631.5:c.123C>T (NCF4) MANE Select	NP_000622.2:p.Phe41=
NM_013416.4:c.123C>T (NCF4)	NP_038202.2:p.Phe41=