Canonical Allele Identifier: CA9269723
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 328440
ClinVar RCV Id: RCV000329180 RCV001590965
dbSNP Id: rs139163760
ExAC: 19:15651463 G / A
gnomAD v2: 19-15651463-G-A
gnomAD v3: 19-15540652-G-A
gnomAD v4: 19-15540652-G-A
COSMIC: COSM1249614
MyVariant Identifiers: chr19:g.15651463G>A (hg19) chr19:g.15540652G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540652G>A , CM000681.2:g.15540652G>A GRCh38
NC_000019.9:g.15651463G>A , CM000681.1:g.15651463G>A GRCh37
NC_000019.8:g.15512463G>A NCBI36
NG_007987.1:g.37128G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.874G>A MANE Select ENSP00000269703.1:p.Glu292Lys
ENST00000269703.7:c.874G>A ENSP00000269703.1:p.Glu292Lys
ENST00000601005.2:c.874G>A ENSP00000469866.1:p.Glu292Lys
NM_173483.3:c.874G>A NP_775754.2:p.Glu292Lys
XM_011527692.1:c.874G>A XP_011525994.1:p.Glu292Lys
XM_011527693.1:c.874G>A XP_011525995.1:p.Glu292Lys
XM_011527692.2:c.874G>A XP_011525994.1:p.Glu292Lys
XM_011527693.2:c.874G>A XP_011525995.1:p.Glu292Lys
NM_173483.4:c.874G>A MANE Select NP_775754.2:p.Glu292Lys
Search 100 bp 5'
Search 100 bp 3'