Canonical Allele Identifier: CA358947497
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197055C>A , CM000666.2:g.186197055C>A GRCh38
NC_000004.11:g.187118209C>A , CM000666.1:g.187118209C>A GRCh37
NC_000004.10:g.187355203C>A NCBI36
NG_007965.1:g.10536C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.529C>A MANE Select ENSP00000368079.4:p.Leu177Ile
ENST00000378802.4:c.529C>A ENSP00000368079.4:p.Leu177Ile
ENST00000507209.5:n.968C>A
NM_207352.3:c.529C>A NP_997235.3:p.Leu177Ile
XM_005262935.2:c.529C>A XP_005262992.1:p.Leu177Ile
XM_006714184.2:c.133C>A XP_006714247.1:p.Leu45Ile
XM_005262935.4:c.529C>A XP_005262992.1:p.Leu177Ile
XM_017008037.1:c.133C>A XP_016863526.1:p.Leu45Ile
NM_207352.4:c.529C>A MANE Select NP_997235.3:p.Leu177Ile