Canonical Allele Identifier: CA1519920435
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198964G= , CM000666.2:g.186198964G= GRCh38
NC_000004.11:g.187120118G= , CM000666.1:g.187120118G= GRCh37
NC_000004.10:g.187357112G= NCBI36
NG_007965.1:g.12445G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.682G= MANE Select ENSP00000368079.4:p.Glu228=
ENST00000378802.4:c.682G= ENSP00000368079.4:p.Glu228=
ENST00000507209.5:n.1523G=
NM_207352.3:c.682G= NP_997235.3:p.Glu228=
XM_005262935.2:c.682G= XP_005262992.1:p.Glu228=
XM_006714184.2:c.286G= XP_006714247.1:p.Glu96=
XM_005262935.4:c.682G= XP_005262992.1:p.Glu228=
XM_017008037.1:c.286G= XP_016863526.1:p.Glu96=
NM_207352.4:c.682G= MANE Select NP_997235.3:p.Glu228=