Canonical Allele Identifier: CA1519919394
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197590G= , CM000666.2:g.186197590G= GRCh38
NC_000004.11:g.187118744G= , CM000666.1:g.187118744G= GRCh37
NC_000004.10:g.187355738G= NCBI36
NG_007965.1:g.11071G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.662G= MANE Select ENSP00000368079.4:p.Arg221=
ENST00000378802.4:c.662G= ENSP00000368079.4:p.Arg221=
ENST00000507209.5:n.1503G=
NM_207352.3:c.662G= NP_997235.3:p.Arg221=
XM_005262935.2:c.662G= XP_005262992.1:p.Arg221=
XM_006714184.2:c.266G= XP_006714247.1:p.Arg89=
XM_005262935.4:c.662G= XP_005262992.1:p.Arg221=
XM_017008037.1:c.266G= XP_016863526.1:p.Arg89=
NM_207352.4:c.662G= MANE Select NP_997235.3:p.Arg221=