Canonical Allele Identifier: CA1519910292

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186191696A= , CM000666.2:g.186191696A=	GRCh38
NC_000004.11:g.187112850A= , CM000666.1:g.187112850A=	GRCh37
NC_000004.10:g.187349844A=	NCBI36
NG_007965.1:g.5177A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.-128A= MANE Select	ENSP00000368079.4:n.-128A=
ENST00000378802.4:c.-128A=	ENSP00000368079.4:n.-128A=
NM_207352.3:c.-128A=	NP_997235.3:n.-128A=
XM_005262935.2:c.-128A=	XP_005262992.1:n.-128A=
XM_017008037.1:c.-438A=	XP_016863526.1:n.-438A=
NM_207352.4:c.-128A= MANE Select	NP_997235.3:n.-128A=