Canonical Allele Identifier: CA9269687
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2228919
ClinVar RCV Id: RCV002692355
dbSNP Id: rs761113998
ExAC: 19:15651320 A / G
gnomAD v2: 19-15651320-A-G
gnomAD v3: 19-15540509-A-G
gnomAD v4: 19-15540509-A-G
MyVariant Identifiers: chr19:g.15651320A>G (hg19) chr19:g.15540509A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540509A>G , CM000681.2:g.15540509A>G GRCh38
NC_000019.9:g.15651320A>G , CM000681.1:g.15651320A>G GRCh37
NC_000019.8:g.15512320A>G NCBI36
NG_007987.1:g.36985A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.731A>G MANE Select ENSP00000269703.1:p.Gln244Arg
ENST00000269703.7:c.731A>G ENSP00000269703.1:p.Gln244Arg
ENST00000601005.2:c.731A>G ENSP00000469866.1:p.Gln244Arg
NM_173483.3:c.731A>G NP_775754.2:p.Gln244Arg
XM_011527692.1:c.731A>G XP_011525994.1:p.Gln244Arg
XM_011527693.1:c.731A>G XP_011525995.1:p.Gln244Arg
XM_011527692.2:c.731A>G XP_011525994.1:p.Gln244Arg
XM_011527693.2:c.731A>G XP_011525995.1:p.Gln244Arg
NM_173483.4:c.731A>G MANE Select NP_775754.2:p.Gln244Arg
Search 100 bp 5'
Search 100 bp 3'