Canonical Allele Identifier: CA1519914663

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194315A= , CM000666.2:g.186194315A=	GRCh38
NC_000004.11:g.187115469A= , CM000666.1:g.187115469A=	GRCh37
NC_000004.10:g.187352463A=	NCBI36
NG_007965.1:g.7796A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.215-185A= MANE Select	ENSP00000368079.4:n.215-185A=
ENST00000378802.4:c.215-185A=	ENSP00000368079.4:n.215-185A=
NM_207352.3:c.215-185A=	NP_997235.3:n.215-185A=
XM_005262935.2:c.215-185A=	XP_005262992.1:n.215-185A=
XM_005262935.4:c.215-185A=	XP_005262992.1:n.215-185A=
XM_017008037.1:c.-96-185A=	XP_016863526.1:n.-96-185A=
NM_207352.4:c.215-185A= MANE Select	NP_997235.3:n.215-185A=