Canonical Allele Identifier: CA505828233
Gene: CYP4F22 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15651436C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540625C>A , CM000681.2:g.15540625C>A GRCh38
NC_000019.9:g.15651436C>A , CM000681.1:g.15651436C>A GRCh37
NC_000019.8:g.15512436C>A NCBI36
NG_007987.1:g.37101C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.847C>A MANE Select ENSP00000269703.1:p.Arg283=
ENST00000269703.7:c.847C>A ENSP00000269703.1:p.Arg283=
ENST00000601005.2:c.847C>A ENSP00000469866.1:p.Arg283=
NM_173483.3:c.847C>A NP_775754.2:p.Arg283=
XM_011527692.1:c.847C>A XP_011525994.1:p.Arg283=
XM_011527693.1:c.847C>A XP_011525995.1:p.Arg283=
XM_011527692.2:c.847C>A XP_011525994.1:p.Arg283=
XM_011527693.2:c.847C>A XP_011525995.1:p.Arg283=
NM_173483.4:c.847C>A MANE Select NP_775754.2:p.Arg283=