Canonical Allele Identifier: CA1519888781

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736455485

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205044dup , CM000666.2:g.186205044dup	GRCh38
NC_000004.11:g.187126198dup , CM000666.1:g.187126198dup	GRCh37
NC_000004.10:g.187363192dup	NCBI36
NG_007965.1:g.18525dup
NG_012095.2:g.1066dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-156dup MANE Select	ENSP00000368079.4:n.988-156dup
ENST00000378802.4:c.988-156dup	ENSP00000368079.4:n.988-156dup
ENST00000502665.1:n.208dup
ENST00000507209.5:n.5530dup
ENST00000513354.5:n.78-156dup
NM_207352.3:c.988-156dup	NP_997235.3:n.988-156dup
XM_005262935.2:c.988-156dup	XP_005262992.1:n.988-156dup
XM_006714184.2:c.592-156dup	XP_006714247.1:n.592-156dup
XM_005262935.4:c.988-156dup	XP_005262992.1:n.988-156dup
XM_017008037.1:c.592-156dup	XP_016863526.1:n.592-156dup
NM_207352.4:c.988-156dup MANE Select	NP_997235.3:n.988-156dup