Canonical Allele Identifier: CA1519920475
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199076C= , CM000666.2:g.186199076C= GRCh38
NC_000004.11:g.187120230C= , CM000666.1:g.187120230C= GRCh37
NC_000004.10:g.187357224C= NCBI36
NG_007965.1:g.12557C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.794C= MANE Select ENSP00000368079.4:p.Thr265=
ENST00000378802.4:c.794C= ENSP00000368079.4:p.Thr265=
ENST00000507209.5:n.1635C=
NM_207352.3:c.794C= NP_997235.3:p.Thr265=
XM_005262935.2:c.794C= XP_005262992.1:p.Thr265=
XM_006714184.2:c.398C= XP_006714247.1:p.Thr133=
XM_005262935.4:c.794C= XP_005262992.1:p.Thr265=
XM_017008037.1:c.398C= XP_016863526.1:p.Thr133=
NM_207352.4:c.794C= MANE Select NP_997235.3:p.Thr265=