Canonical Allele Identifier: CA404536115
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs1295378293

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540644A>C , CM000681.2:g.15540644A>C GRCh38
NC_000019.9:g.15651455A>C , CM000681.1:g.15651455A>C GRCh37
NC_000019.8:g.15512455A>C NCBI36
NG_007987.1:g.37120A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.866A>C MANE Select ENSP00000269703.1:p.Gln289Pro
ENST00000269703.7:c.866A>C ENSP00000269703.1:p.Gln289Pro
ENST00000601005.2:c.866A>C ENSP00000469866.1:p.Gln289Pro
NM_173483.3:c.866A>C NP_775754.2:p.Gln289Pro
XM_011527692.1:c.866A>C XP_011525994.1:p.Gln289Pro
XM_011527693.1:c.866A>C XP_011525995.1:p.Gln289Pro
XM_011527692.2:c.866A>C XP_011525994.1:p.Gln289Pro
XM_011527693.2:c.866A>C XP_011525995.1:p.Gln289Pro
NM_173483.4:c.866A>C MANE Select NP_775754.2:p.Gln289Pro