Canonical Allele Identifier: CA323982620

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs562165010
• gnomAD v2: 22-37258576-C-T
• gnomAD v3: 22-36862534-C-T
• gnomAD v4: 22-36862534-C-T
• MyVariant Identifiers: chr22:g.37258576C>T (hg19) ; chr22:g.36862534C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862534C>T , CM000684.2:g.36862534C>T	GRCh38
NC_000022.10:g.37258576C>T , CM000684.1:g.37258576C>T	GRCh37
NC_000022.9:g.35588522C>T	NCBI36
NG_023400.1:g.6547C>T , LRG_159:g.6547C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.32+1331C>T (NCF4) MANE Select	ENSP00000248899.6:n.32+1331C>T
ENST00000397147.7:c.32+1331C>T (NCF4)	ENSP00000380334.4:n.32+1331C>T
ENST00000650827.1:c.-278+147C>T (NCF4)	ENSP00000498212.1:n.-278+147C>T
ENST00000651053.1:n.11C>T (NCF4)
ENST00000248899.10:c.32+1331C>T (NCF4)	ENSP00000248899.6:n.32+1331C>T
ENST00000397147.6:c.32+1331C>T (NCF4)	ENSP00000380334.4:n.32+1331C>T
ENST00000447071.5:c.-193+1331C>T (NCF4)	ENSP00000414958.1:n.-193+1331C>T
NM_000631.4:c.32+1331C>T (NCF4)	NP_000622.2:n.32+1331C>T
NM_013416.3:c.32+1331C>T , LRG_159t1:c.32+1331C>T (NCF4)	NP_038202.2:n.32+1331C>T
XM_011530198.1:c.-121C>T (NCF4)	XP_011528500.1:n.-121C>T
XM_011530199.1:c.98-613C>T (NCF4)	XP_011528501.1:n.98-613C>T
NR_147197.1:n.351+7559G>A (NCF4-AS1)
XM_017028808.1:c.-278+719C>T (NCF4)	XP_016884297.1:n.-278+719C>T
NM_000631.5:c.32+1331C>T (NCF4) MANE Select	NP_000622.2:n.32+1331C>T
NM_013416.4:c.32+1331C>T (NCF4)	NP_038202.2:n.32+1331C>T