Canonical Allele Identifier: CA1519920458
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199038G= , CM000666.2:g.186199038G= GRCh38
NC_000004.11:g.187120192G= , CM000666.1:g.187120192G= GRCh37
NC_000004.10:g.187357186G= NCBI36
NG_007965.1:g.12519G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.756G= MANE Select ENSP00000368079.4:p.Trp252=
ENST00000378802.4:c.756G= ENSP00000368079.4:p.Trp252=
ENST00000507209.5:n.1597G=
NM_207352.3:c.756G= NP_997235.3:p.Trp252=
XM_005262935.2:c.756G= XP_005262992.1:p.Trp252=
XM_006714184.2:c.360G= XP_006714247.1:p.Trp120=
XM_005262935.4:c.756G= XP_005262992.1:p.Trp252=
XM_017008037.1:c.360G= XP_016863526.1:p.Trp120=
NM_207352.4:c.756G= MANE Select NP_997235.3:p.Trp252=