Canonical Allele Identifier: CA305826386
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs772654580

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540634C>G , CM000681.2:g.15540634C>G GRCh38
NC_000019.9:g.15651445C>G , CM000681.1:g.15651445C>G GRCh37
NC_000019.8:g.15512445C>G NCBI36
NG_007987.1:g.37110C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.856C>G MANE Select ENSP00000269703.1:p.Leu286Val
ENST00000269703.7:c.856C>G ENSP00000269703.1:p.Leu286Val
ENST00000601005.2:c.856C>G ENSP00000469866.1:p.Leu286Val
NM_173483.3:c.856C>G NP_775754.2:p.Leu286Val
XM_011527692.1:c.856C>G XP_011525994.1:p.Leu286Val
XM_011527693.1:c.856C>G XP_011525995.1:p.Leu286Val
XM_011527692.2:c.856C>G XP_011525994.1:p.Leu286Val
XM_011527693.2:c.856C>G XP_011525995.1:p.Leu286Val
NM_173483.4:c.856C>G MANE Select NP_775754.2:p.Leu286Val