Canonical Allele Identifier: CA1519888902

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736460300

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205168G>A , CM000666.2:g.186205168G>A	GRCh38
NC_000004.11:g.187126322G>A , CM000666.1:g.187126322G>A	GRCh37
NC_000004.10:g.187363316G>A	NCBI36
NG_007965.1:g.18649G>A
NG_012095.2:g.1190G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-32G>A MANE Select	ENSP00000368079.4:n.988-32G>A
ENST00000378802.4:c.988-32G>A	ENSP00000368079.4:n.988-32G>A
ENST00000502665.1:n.223-32G>A
ENST00000507209.5:n.5654G>A
ENST00000513354.5:n.78-32G>A
NM_207352.3:c.988-32G>A	NP_997235.3:n.988-32G>A
XM_005262935.2:c.988-32G>A	XP_005262992.1:n.988-32G>A
XM_006714184.2:c.592-32G>A	XP_006714247.1:n.592-32G>A
XM_005262935.4:c.988-32G>A	XP_005262992.1:n.988-32G>A
XM_017008037.1:c.592-32G>A	XP_016863526.1:n.592-32G>A
NM_207352.4:c.988-32G>A MANE Select	NP_997235.3:n.988-32G>A