Canonical Allele Identifier: CA1519920481
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199093T= , CM000666.2:g.186199093T= GRCh38
NC_000004.11:g.187120247T= , CM000666.1:g.187120247T= GRCh37
NC_000004.10:g.187357241T= NCBI36
NG_007965.1:g.12574T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+10T= MANE Select ENSP00000368079.4:n.801+10T=
ENST00000378802.4:c.801+10T= ENSP00000368079.4:n.801+10T=
ENST00000507209.5:n.1642+10T=
NM_207352.3:c.801+10T= NP_997235.3:n.801+10T=
XM_005262935.2:c.801+10T= XP_005262992.1:n.801+10T=
XM_006714184.2:c.405+10T= XP_006714247.1:n.405+10T=
XM_005262935.4:c.801+10T= XP_005262992.1:n.801+10T=
XM_017008037.1:c.405+10T= XP_016863526.1:n.405+10T=
NM_207352.4:c.801+10T= MANE Select NP_997235.3:n.801+10T=