Canonical Allele Identifier: CA9269637
Gene: CYP4F22 HGNC NCBI
COSMIC:
COSM1129964 (not active)
MyVariant.info:
GRCh38 chr19:g.15537904G>A
GRCh37 chr19:g.15648715G>A
gnomAD v2:
19:15648715 G / A
gnomAD v3:
19:15537904 G / A
gnomAD v4:
chr19-15537904-G-A
Joint Max Group AF 0.12421487 (MID)
Genomes Max Group AF 0.11413943 (NFE)
Exomes Max Group AF 0.12381323 (MID)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15537904G>A , CM000681.2:g.15537904G>A GRCh38
NC_000019.9:g.15648715G>A , CM000681.1:g.15648715G>A GRCh37
NC_000019.8:g.15509715G>A NCBI36
NG_007987.1:g.34380G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.582G>A MANE Select ENSP00000269703.1:p.Ala194=
ENST00000269703.7:c.582G>A ENSP00000269703.1:p.Ala194=
ENST00000601005.2:c.582G>A ENSP00000469866.1:p.Ala194=
NM_173483.3:c.582G>A NP_775754.2:p.Ala194=
XM_011527692.1:c.582G>A XP_011525994.1:p.Ala194=
XM_011527693.1:c.582G>A XP_011525995.1:p.Ala194=
XM_011527692.2:c.582G>A XP_011525994.1:p.Ala194=
XM_011527693.2:c.582G>A XP_011525995.1:p.Ala194=
NM_173483.4:c.582G>A MANE Select NP_775754.2:p.Ala194=
Search 100 bp 5'
Search 100 bp 3'