Canonical Allele Identifier: CA114618
Gene: CYP4F22 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 911
ClinVar RCV Id: RCV000000959
dbSNP Id: rs118203937

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540506G>A , CM000681.2:g.15540506G>A GRCh38
NC_000019.8:g.15512317G>A NCBI36
NC_000019.9:g.15651317G>A , CM000681.1:g.15651317G>A GRCh37
NG_007987.1:g.36982G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.7:c.728G>A ENSP00000269703.1:p.Arg243His
ENST00000601005.2:c.728G>A ENSP00000469866.1:p.Arg243His
NM_173483.3:c.728G>A NP_775754.2:p.Arg243His
XM_011527692.1:c.728G>A XP_011525994.1:p.Arg243His
XM_011527693.1:c.728G>A XP_011525995.1:p.Arg243His