Canonical Allele Identifier: CA2764868515

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200649G>A , CM000666.2:g.186200649G>A	GRCh38
NC_000004.11:g.187121803G>A , CM000666.1:g.187121803G>A	GRCh37
NC_000004.10:g.187358797G>A	NCBI36
NG_007965.1:g.14130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-508G>A MANE Select	ENSP00000368079.4:n.802-508G>A
ENST00000378802.4:c.802-508G>A	ENSP00000368079.4:n.802-508G>A
ENST00000507209.5:n.1643-508G>A
NM_207352.3:c.802-508G>A	NP_997235.3:n.802-508G>A
XM_005262935.2:c.802-508G>A	XP_005262992.1:n.802-508G>A
XM_006714184.2:c.406-508G>A	XP_006714247.1:n.406-508G>A
XM_005262935.4:c.802-508G>A	XP_005262992.1:n.802-508G>A
XM_017008037.1:c.406-508G>A	XP_016863526.1:n.406-508G>A
NM_207352.4:c.802-508G>A MANE Select	NP_997235.3:n.802-508G>A