Canonical Allele Identifier: CA442640963

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186205238-A-G
• MyVariant Identifiers: chr4:g.187126392A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205238A>G , CM000666.2:g.186205238A>G	GRCh38
NC_000004.11:g.187126392A>G , CM000666.1:g.187126392A>G	GRCh37
NC_000004.10:g.187363386A>G	NCBI36
NG_007965.1:g.18719A>G
NG_012095.2:g.1260A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1026A>G MANE Select	ENSP00000368079.4:p.Leu342=
ENST00000378802.4:c.1026A>G	ENSP00000368079.4:p.Leu342=
ENST00000502665.1:n.261A>G
ENST00000507209.5:n.5724A>G
ENST00000513354.5:n.116A>G
NM_207352.3:c.1026A>G	NP_997235.3:p.Leu342=
XM_005262935.2:c.1026A>G	XP_005262992.1:p.Leu342=
XM_006714184.2:c.630A>G	XP_006714247.1:p.Leu210=
XM_005262935.4:c.1026A>G	XP_005262992.1:p.Leu342=
XM_017008037.1:c.630A>G	XP_016863526.1:p.Leu210=
NM_207352.4:c.1026A>G MANE Select	NP_997235.3:p.Leu342=