Canonical Allele Identifier: CA404535807
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540569T>G , CM000681.2:g.15540569T>G GRCh38
NC_000019.9:g.15651380T>G , CM000681.1:g.15651380T>G GRCh37
NC_000019.8:g.15512380T>G NCBI36
NG_007987.1:g.37045T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.791T>G MANE Select ENSP00000269703.1:p.Phe264Cys
ENST00000269703.7:c.791T>G ENSP00000269703.1:p.Phe264Cys
ENST00000601005.2:c.791T>G ENSP00000469866.1:p.Phe264Cys
NM_173483.3:c.791T>G NP_775754.2:p.Phe264Cys
XM_011527692.1:c.791T>G XP_011525994.1:p.Phe264Cys
XM_011527693.1:c.791T>G XP_011525995.1:p.Phe264Cys
XM_011527692.2:c.791T>G XP_011525994.1:p.Phe264Cys
XM_011527693.2:c.791T>G XP_011525995.1:p.Phe264Cys
NM_173483.4:c.791T>G MANE Select NP_775754.2:p.Phe264Cys