Canonical Allele Identifier: CA1519884286
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186201152T= , CM000666.2:g.186201152T= GRCh38
NC_000004.11:g.187122306T= , CM000666.1:g.187122306T= GRCh37
NC_000004.10:g.187359300T= NCBI36
NG_007965.1:g.14633T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.802-5T= MANE Select ENSP00000368079.4:n.802-5T=
ENST00000378802.4:c.802-5T= ENSP00000368079.4:n.802-5T=
ENST00000507209.5:n.1643-5T=
NM_207352.3:c.802-5T= NP_997235.3:n.802-5T=
XM_005262935.2:c.802-5T= XP_005262992.1:n.802-5T=
XM_006714184.2:c.406-5T= XP_006714247.1:n.406-5T=
XM_005262935.4:c.802-5T= XP_005262992.1:n.802-5T=
XM_017008037.1:c.406-5T= XP_016863526.1:n.406-5T=
NM_207352.4:c.802-5T= MANE Select NP_997235.3:n.802-5T=