Canonical Allele Identifier: CA1519915226
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194608T= , CM000666.2:g.186194608T= GRCh38
NC_000004.11:g.187115762T= , CM000666.1:g.187115762T= GRCh37
NC_000004.10:g.187352756T= NCBI36
NG_007965.1:g.8089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.323T= MANE Select ENSP00000368079.4:p.Val108=
ENST00000378802.4:c.323T= ENSP00000368079.4:p.Val108=
NM_207352.3:c.323T= NP_997235.3:p.Val108=
XM_005262935.2:c.323T= XP_005262992.1:p.Val108=
XM_006714184.2:c.13T= XP_006714247.1:p.Trp5=
XM_005262935.4:c.323T= XP_005262992.1:p.Val108=
XM_017008037.1:c.13T= XP_016863526.1:p.Trp5=
NM_207352.4:c.323T= MANE Select NP_997235.3:p.Val108=