Canonical Allele Identifier: CA9269526

Gene: CYP4F22

Linked Data

• ClinVar Variation Id: 328426
• ClinVar RCV Id: RCV000309690 ; RCV001653595
• dbSNP Id: rs73512652
• ExAC: 19:15640669 G / A
• gnomAD v2: 19-15640669-G-A
• gnomAD v3: 19-15529858-G-A
• gnomAD v4: 19-15529858-G-A
• MyVariant Identifiers: chr19:g.15640669G>A (hg19) ; chr19:g.15529858G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15529858G>A , CM000681.2:g.15529858G>A	GRCh38
NC_000019.9:g.15640669G>A , CM000681.1:g.15640669G>A	GRCh37
NC_000019.8:g.15501669G>A	NCBI36
NG_007987.1:g.26334G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.367+5G>A MANE Select	ENSP00000269703.1:n.367+5G>A
ENST00000269703.7:c.367+5G>A	ENSP00000269703.1:n.367+5G>A
ENST00000601005.2:c.367+5G>A	ENSP00000469866.1:n.367+5G>A
NM_173483.3:c.367+5G>A	NP_775754.2:n.367+5G>A
XM_011527692.1:c.367+5G>A	XP_011525994.1:n.367+5G>A
XM_011527693.1:c.367+5G>A	XP_011525995.1:n.367+5G>A
XM_011527692.2:c.367+5G>A	XP_011525994.1:n.367+5G>A
XM_011527693.2:c.367+5G>A	XP_011525995.1:n.367+5G>A
NM_173483.4:c.367+5G>A MANE Select	NP_775754.2:n.367+5G>A