Canonical Allele Identifier: CA343726
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39261
ClinVar RCV Id: RCV000032538
dbSNP Id: rs199476187

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194568G>A , CM000666.2:g.186194568G>A GRCh38
NC_000004.11:g.187115722G>A , CM000666.1:g.187115722G>A GRCh37
NC_000004.10:g.187352716G>A NCBI36
NG_007965.1:g.8049G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.283G>A MANE Select ENSP00000368079.4:p.Gly95Arg
ENST00000378802.4:c.283G>A ENSP00000368079.4:p.Gly95Arg
NM_207352.3:c.283G>A NP_997235.3:p.Gly95Arg
XM_005262935.2:c.283G>A XP_005262992.1:p.Gly95Arg
XM_006714184.2:c.-28G>A XP_006714247.1:p.=
XM_005262935.4:c.283G>A XP_005262992.1:p.Gly95Arg
XM_017008037.1:c.-28G>A XP_016863526.1:p.=
NM_207352.4:c.283G>A MANE Select NP_997235.3:p.Gly95Arg