Canonical Allele Identifier: CA2672896366

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204862-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204862G>T , CM000666.2:g.186204862G>T	GRCh38
NC_000004.11:g.187126016G>T , CM000666.1:g.187126016G>T	GRCh37
NC_000004.10:g.187363010G>T	NCBI36
NG_007965.1:g.18343G>T
NG_012095.2:g.884G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-338G>T MANE Select	ENSP00000368079.4:n.988-338G>T
ENST00000378802.4:c.988-338G>T	ENSP00000368079.4:n.988-338G>T
ENST00000502665.1:n.26G>T
ENST00000507209.5:n.5348G>T
ENST00000513354.5:n.78-338G>T
NM_207352.3:c.988-338G>T	NP_997235.3:n.988-338G>T
XM_005262935.2:c.988-338G>T	XP_005262992.1:n.988-338G>T
XM_006714184.2:c.592-338G>T	XP_006714247.1:n.592-338G>T
XM_005262935.4:c.988-338G>T	XP_005262992.1:n.988-338G>T
XM_017008037.1:c.592-338G>T	XP_016863526.1:n.592-338G>T
NM_207352.4:c.988-338G>T MANE Select	NP_997235.3:n.988-338G>T