Canonical Allele Identifier: CA358946945
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194569G>A , CM000666.2:g.186194569G>A GRCh38
NC_000004.11:g.187115723G>A , CM000666.1:g.187115723G>A GRCh37
NC_000004.10:g.187352717G>A NCBI36
NG_007965.1:g.8050G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.284G>A MANE Select ENSP00000368079.4:p.Gly95Glu
ENST00000378802.4:c.284G>A ENSP00000368079.4:p.Gly95Glu
NM_207352.3:c.284G>A NP_997235.3:p.Gly95Glu
XM_005262935.2:c.284G>A XP_005262992.1:p.Gly95Glu
XM_006714184.2:c.-27G>A XP_006714247.1:p.=
XM_005262935.4:c.284G>A XP_005262992.1:p.Gly95Glu
XM_017008037.1:c.-27G>A XP_016863526.1:p.=
NM_207352.4:c.284G>A MANE Select NP_997235.3:p.Gly95Glu