Canonical Allele Identifier: CA404536203
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540662T>A , CM000681.2:g.15540662T>A GRCh38
NC_000019.9:g.15651473T>A , CM000681.1:g.15651473T>A GRCh37
NC_000019.8:g.15512473T>A NCBI36
NG_007987.1:g.37138T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.884T>A MANE Select ENSP00000269703.1:p.Leu295His
ENST00000269703.7:c.884T>A ENSP00000269703.1:p.Leu295His
ENST00000601005.2:c.884T>A ENSP00000469866.1:p.Leu295His
NM_173483.3:c.884T>A NP_775754.2:p.Leu295His
XM_011527692.1:c.884T>A XP_011525994.1:p.Leu295His
XM_011527693.1:c.884T>A XP_011525995.1:p.Leu295His
XM_011527692.2:c.884T>A XP_011525994.1:p.Leu295His
XM_011527693.2:c.884T>A XP_011525995.1:p.Leu295His
NM_173483.4:c.884T>A MANE Select NP_775754.2:p.Leu295His