Canonical Allele Identifier: CA1519915012

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194528A= , CM000666.2:g.186194528A=	GRCh38
NC_000004.11:g.187115682A= , CM000666.1:g.187115682A=	GRCh37
NC_000004.10:g.187352676A=	NCBI36
NG_007965.1:g.8009A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.243A= MANE Select	ENSP00000368079.4:p.Thr81=
ENST00000378802.4:c.243A=	ENSP00000368079.4:p.Thr81=
NM_207352.3:c.243A=	NP_997235.3:p.Thr81=
XM_005262935.2:c.243A=	XP_005262992.1:p.Thr81=
XM_006714184.2:c.-68A=	XP_006714247.1:n.-68A=
XM_005262935.4:c.243A=	XP_005262992.1:p.Thr81=
XM_017008037.1:c.-68A=	XP_016863526.1:n.-68A=
NM_207352.4:c.243A= MANE Select	NP_997235.3:p.Thr81=