Canonical Allele Identifier: CA752887825

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs1303274681
• gnomAD v3: 22-36862341-G-C
• gnomAD v4: 22-36862341-G-C
• MyVariant Identifiers: chr22:g.37258383G>C (hg19) ; chr22:g.36862341G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862341G>C , CM000684.2:g.36862341G>C	GRCh38
NC_000022.10:g.37258383G>C , CM000684.1:g.37258383G>C	GRCh37
NC_000022.9:g.35588329G>C	NCBI36
NG_023400.1:g.6354G>C , LRG_159:g.6354G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.32+1138G>C (NCF4) MANE Select	ENSP00000248899.6:n.32+1138G>C
ENST00000397147.7:c.32+1138G>C (NCF4)	ENSP00000380334.4:n.32+1138G>C
ENST00000650827.1:c.-324G>C (NCF4)	ENSP00000498212.1:n.-324G>C
ENST00000248899.10:c.32+1138G>C (NCF4)	ENSP00000248899.6:n.32+1138G>C
ENST00000397147.6:c.32+1138G>C (NCF4)	ENSP00000380334.4:n.32+1138G>C
ENST00000447071.5:c.-193+1138G>C (NCF4)	ENSP00000414958.1:n.-193+1138G>C
NM_000631.4:c.32+1138G>C (NCF4)	NP_000622.2:n.32+1138G>C
NM_013416.3:c.32+1138G>C , LRG_159t1:c.32+1138G>C (NCF4)	NP_038202.2:n.32+1138G>C
XM_011530198.1:c.-314G>C (NCF4)	XP_011528500.1:n.-314G>C
XM_011530199.1:c.97+526G>C (NCF4)	XP_011528501.1:n.97+526G>C
NR_147197.1:n.351+7752C>G (NCF4-AS1)
XM_017028808.1:c.-278+526G>C (NCF4)	XP_016884297.1:n.-278+526G>C
NM_000631.5:c.32+1138G>C (NCF4) MANE Select	NP_000622.2:n.32+1138G>C
NM_013416.4:c.32+1138G>C (NCF4)	NP_038202.2:n.32+1138G>C