Canonical Allele Identifier: CA1519888885
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205155G= , CM000666.2:g.186205155G= GRCh38
NC_000004.11:g.187126309G= , CM000666.1:g.187126309G= GRCh37
NC_000004.10:g.187363303G= NCBI36
NG_007965.1:g.18636G=
NG_012095.2:g.1177G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-45G= MANE Select ENSP00000368079.4:n.988-45G=
ENST00000378802.4:c.988-45G= ENSP00000368079.4:n.988-45G=
ENST00000502665.1:n.223-45G=
ENST00000507209.5:n.5641G=
ENST00000513354.5:n.78-45G=
NM_207352.3:c.988-45G= NP_997235.3:n.988-45G=
XM_005262935.2:c.988-45G= XP_005262992.1:n.988-45G=
XM_006714184.2:c.592-45G= XP_006714247.1:n.592-45G=
XM_005262935.4:c.988-45G= XP_005262992.1:n.988-45G=
XM_017008037.1:c.592-45G= XP_016863526.1:n.592-45G=
NM_207352.4:c.988-45G= MANE Select NP_997235.3:n.988-45G=