Canonical Allele Identifier: CA2672896819

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186205089-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205089C>A , CM000666.2:g.186205089C>A	GRCh38
NC_000004.11:g.187126243C>A , CM000666.1:g.187126243C>A	GRCh37
NC_000004.10:g.187363237C>A	NCBI36
NG_007965.1:g.18570C>A
NG_012095.2:g.1111C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-111C>A MANE Select	ENSP00000368079.4:n.988-111C>A
ENST00000378802.4:c.988-111C>A	ENSP00000368079.4:n.988-111C>A
ENST00000502665.1:n.222+31C>A
ENST00000507209.5:n.5575C>A
ENST00000513354.5:n.78-111C>A
NM_207352.3:c.988-111C>A	NP_997235.3:n.988-111C>A
XM_005262935.2:c.988-111C>A	XP_005262992.1:n.988-111C>A
XM_006714184.2:c.592-111C>A	XP_006714247.1:n.592-111C>A
XM_005262935.4:c.988-111C>A	XP_005262992.1:n.988-111C>A
XM_017008037.1:c.592-111C>A	XP_016863526.1:n.592-111C>A
NM_207352.4:c.988-111C>A MANE Select	NP_997235.3:n.988-111C>A