Canonical Allele Identifier: CA1519914642

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194278G= , CM000666.2:g.186194278G=	GRCh38
NC_000004.11:g.187115432G= , CM000666.1:g.187115432G=	GRCh37
NC_000004.10:g.187352426G=	NCBI36
NG_007965.1:g.7759G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.215-222G= MANE Select	ENSP00000368079.4:n.215-222G=
ENST00000378802.4:c.215-222G=	ENSP00000368079.4:n.215-222G=
NM_207352.3:c.215-222G=	NP_997235.3:n.215-222G=
XM_005262935.2:c.215-222G=	XP_005262992.1:n.215-222G=
XM_005262935.4:c.215-222G=	XP_005262992.1:n.215-222G=
XM_017008037.1:c.-96-222G=	XP_016863526.1:n.-96-222G=
NM_207352.4:c.215-222G= MANE Select	NP_997235.3:n.215-222G=