Canonical Allele Identifier: CA404536327
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651502T>A (hg19) chr19:g.15540691T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540691T>A , CM000681.2:g.15540691T>A GRCh38
NC_000019.9:g.15651502T>A , CM000681.1:g.15651502T>A GRCh37
NC_000019.8:g.15512502T>A NCBI36
NG_007987.1:g.37167T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.913T>A MANE Select ENSP00000269703.1:p.Phe305Ile
ENST00000269703.7:c.913T>A ENSP00000269703.1:p.Phe305Ile
ENST00000601005.2:c.913T>A ENSP00000469866.1:p.Phe305Ile
NM_173483.3:c.913T>A NP_775754.2:p.Phe305Ile
XM_011527692.1:c.913T>A XP_011525994.1:p.Phe305Ile
XM_011527693.1:c.913T>A XP_011525995.1:p.Phe305Ile
XM_011527692.2:c.913T>A XP_011525994.1:p.Phe305Ile
XM_011527693.2:c.913T>A XP_011525995.1:p.Phe305Ile
NM_173483.4:c.913T>A MANE Select NP_775754.2:p.Phe305Ile
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