Canonical Allele Identifier: CA358947295

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187118120G>T (hg19) ; chr4:g.186196966G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186196966G>T , CM000666.2:g.186196966G>T	GRCh38
NC_000004.11:g.187118120G>T , CM000666.1:g.187118120G>T	GRCh37
NC_000004.10:g.187355114G>T	NCBI36
NG_007965.1:g.10447G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.440G>T MANE Select	ENSP00000368079.4:p.Arg147Ile
ENST00000378802.4:c.440G>T	ENSP00000368079.4:p.Arg147Ile
ENST00000507209.5:n.879G>T
NM_207352.3:c.440G>T	NP_997235.3:p.Arg147Ile
XM_005262935.2:c.440G>T	XP_005262992.1:p.Arg147Ile
XM_006714184.2:c.44G>T	XP_006714247.1:p.Arg15Ile
XM_005262935.4:c.440G>T	XP_005262992.1:p.Arg147Ile
XM_017008037.1:c.44G>T	XP_016863526.1:p.Arg15Ile
NM_207352.4:c.440G>T MANE Select	NP_997235.3:p.Arg147Ile