Canonical Allele Identifier: CA1519916953

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186195960T= , CM000666.2:g.186195960T=	GRCh38
NC_000004.11:g.187117114T= , CM000666.1:g.187117114T=	GRCh37
NC_000004.10:g.187354108T=	NCBI36
NG_007965.1:g.9441T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.328-43T= MANE Select	ENSP00000368079.4:n.328-43T=
ENST00000378802.4:c.328-43T=	ENSP00000368079.4:n.328-43T=
NM_207352.3:c.328-43T=	NP_997235.3:n.328-43T=
XM_005262935.2:c.328-43T=	XP_005262992.1:n.328-43T=
XM_006714184.2:c.18-980T=	XP_006714247.1:n.18-980T=
XM_005262935.4:c.328-43T=	XP_005262992.1:n.328-43T=
XM_017008037.1:c.18-980T=	XP_016863526.1:n.18-980T=
NM_207352.4:c.328-43T= MANE Select	NP_997235.3:n.328-43T=