Canonical Allele Identifier: CA323982619

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs1037168849
• gnomAD v3: 22-36862533-A-G
• gnomAD v4: 22-36862533-A-G
• MyVariant Identifiers: chr22:g.37258575A>G (hg19) ; chr22:g.36862533A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862533A>G , CM000684.2:g.36862533A>G	GRCh38
NC_000022.10:g.37258575A>G , CM000684.1:g.37258575A>G	GRCh37
NC_000022.9:g.35588521A>G	NCBI36
NG_023400.1:g.6546A>G , LRG_159:g.6546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.32+1330A>G (NCF4) MANE Select	ENSP00000248899.6:n.32+1330A>G
ENST00000397147.7:c.32+1330A>G (NCF4)	ENSP00000380334.4:n.32+1330A>G
ENST00000650827.1:c.-278+146A>G (NCF4)	ENSP00000498212.1:n.-278+146A>G
ENST00000651053.1:n.10A>G (NCF4)
ENST00000248899.10:c.32+1330A>G (NCF4)	ENSP00000248899.6:n.32+1330A>G
ENST00000397147.6:c.32+1330A>G (NCF4)	ENSP00000380334.4:n.32+1330A>G
ENST00000447071.5:c.-193+1330A>G (NCF4)	ENSP00000414958.1:n.-193+1330A>G
NM_000631.4:c.32+1330A>G (NCF4)	NP_000622.2:n.32+1330A>G
NM_013416.3:c.32+1330A>G , LRG_159t1:c.32+1330A>G (NCF4)	NP_038202.2:n.32+1330A>G
XM_011530198.1:c.-122A>G (NCF4)	XP_011528500.1:n.-122A>G
XM_011530199.1:c.98-614A>G (NCF4)	XP_011528501.1:n.98-614A>G
NR_147197.1:n.351+7560T>C (NCF4-AS1)
XM_017028808.1:c.-278+718A>G (NCF4)	XP_016884297.1:n.-278+718A>G
NM_000631.5:c.32+1330A>G (NCF4) MANE Select	NP_000622.2:n.32+1330A>G
NM_013416.4:c.32+1330A>G (NCF4)	NP_038202.2:n.32+1330A>G