Canonical Allele Identifier: CA9269728
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs761198340

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540677G>A , CM000681.2:g.15540677G>A GRCh38
NC_000019.9:g.15651488G>A , CM000681.1:g.15651488G>A GRCh37
NC_000019.8:g.15512488G>A NCBI36
NG_007987.1:g.37153G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.899G>A MANE Select ENSP00000269703.1:p.Gly300Glu
ENST00000269703.7:c.899G>A ENSP00000269703.1:p.Gly300Glu
ENST00000601005.2:c.899G>A ENSP00000469866.1:p.Gly300Glu
NM_173483.3:c.899G>A NP_775754.2:p.Gly300Glu
XM_011527692.1:c.899G>A XP_011525994.1:p.Gly300Glu
XM_011527693.1:c.899G>A XP_011525995.1:p.Gly300Glu
XM_011527692.2:c.899G>A XP_011525994.1:p.Gly300Glu
XM_011527693.2:c.899G>A XP_011525995.1:p.Gly300Glu
NM_173483.4:c.899G>A MANE Select NP_775754.2:p.Gly300Glu