Canonical Allele Identifier: CA404535668
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540536T>A , CM000681.2:g.15540536T>A GRCh38
NC_000019.9:g.15651347T>A , CM000681.1:g.15651347T>A GRCh37
NC_000019.8:g.15512347T>A NCBI36
NG_007987.1:g.37012T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.758T>A MANE Select ENSP00000269703.1:p.Phe253Tyr
ENST00000269703.7:c.758T>A ENSP00000269703.1:p.Phe253Tyr
ENST00000601005.2:c.758T>A ENSP00000469866.1:p.Phe253Tyr
NM_173483.3:c.758T>A NP_775754.2:p.Phe253Tyr
XM_011527692.1:c.758T>A XP_011525994.1:p.Phe253Tyr
XM_011527693.1:c.758T>A XP_011525995.1:p.Phe253Tyr
XM_011527692.2:c.758T>A XP_011525994.1:p.Phe253Tyr
XM_011527693.2:c.758T>A XP_011525995.1:p.Phe253Tyr
NM_173483.4:c.758T>A MANE Select NP_775754.2:p.Phe253Tyr