Canonical Allele Identifier: CA1519918483
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197021C= , CM000666.2:g.186197021C= GRCh38
NC_000004.11:g.187118175C= , CM000666.1:g.187118175C= GRCh37
NC_000004.10:g.187355169C= NCBI36
NG_007965.1:g.10502C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.495C= MANE Select ENSP00000368079.4:p.Ile165=
ENST00000378802.4:c.495C= ENSP00000368079.4:p.Ile165=
ENST00000507209.5:n.934C=
NM_207352.3:c.495C= NP_997235.3:p.Ile165=
XM_005262935.2:c.495C= XP_005262992.1:p.Ile165=
XM_006714184.2:c.99C= XP_006714247.1:p.Ile33=
XM_005262935.4:c.495C= XP_005262992.1:p.Ile165=
XM_017008037.1:c.99C= XP_016863526.1:p.Ile33=
NM_207352.4:c.495C= MANE Select NP_997235.3:p.Ile165=