Canonical Allele Identifier: CA1519915236
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194611A= , CM000666.2:g.186194611A= GRCh38
NC_000004.11:g.187115765A= , CM000666.1:g.187115765A= GRCh37
NC_000004.10:g.187352759A= NCBI36
NG_007965.1:g.8092A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.326A= MANE Select ENSP00000368079.4:p.Glu109=
ENST00000378802.4:c.326A= ENSP00000368079.4:p.Glu109=
NM_207352.3:c.326A= NP_997235.3:p.Glu109=
XM_005262935.2:c.326A= XP_005262992.1:p.Glu109=
XM_006714184.2:c.16A= XP_006714247.1:p.Ser6=
XM_005262935.4:c.326A= XP_005262992.1:p.Glu109=
XM_017008037.1:c.16A= XP_016863526.1:p.Ser6=
NM_207352.4:c.326A= MANE Select NP_997235.3:p.Glu109=