Canonical Allele Identifier: CA1519891177

Gene: CYP4V2

Linked Data

• dbSNP Id: rs111537571

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208679A>T , CM000666.2:g.186208679A>T	GRCh38
NC_000004.11:g.187129833A>T , CM000666.1:g.187129833A>T	GRCh37
NC_000004.10:g.187366827A>T	NCBI36
NG_007965.1:g.22160A>T
NG_012095.2:g.4701A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-186A>T MANE Select	ENSP00000368079.4:n.1091-186A>T
ENST00000378802.4:c.1091-186A>T	ENSP00000368079.4:n.1091-186A>T
ENST00000502665.1:n.326-186A>T
ENST00000507209.5:n.5789-186A>T
ENST00000513354.5:n.181-186A>T
NM_207352.3:c.1091-186A>T	NP_997235.3:n.1091-186A>T
XM_005262935.2:c.1091-186A>T	XP_005262992.1:n.1091-186A>T
XM_006714184.2:c.695-186A>T	XP_006714247.1:n.695-186A>T
XM_005262935.4:c.1091-186A>T	XP_005262992.1:n.1091-186A>T
XM_017008037.1:c.695-186A>T	XP_016863526.1:n.695-186A>T
NM_207352.4:c.1091-186A>T MANE Select	NP_997235.3:n.1091-186A>T