Canonical Allele Identifier: CA2764868394

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199158A>T , CM000666.2:g.186199158A>T	GRCh38
NC_000004.11:g.187120312A>T , CM000666.1:g.187120312A>T	GRCh37
NC_000004.10:g.187357306A>T	NCBI36
NG_007965.1:g.12639A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.801+75A>T MANE Select	ENSP00000368079.4:n.801+75A>T
ENST00000378802.4:c.801+75A>T	ENSP00000368079.4:n.801+75A>T
ENST00000507209.5:n.1642+75A>T
NM_207352.3:c.801+75A>T	NP_997235.3:n.801+75A>T
XM_005262935.2:c.801+75A>T	XP_005262992.1:n.801+75A>T
XM_006714184.2:c.405+75A>T	XP_006714247.1:n.405+75A>T
XM_005262935.4:c.801+75A>T	XP_005262992.1:n.801+75A>T
XM_017008037.1:c.405+75A>T	XP_016863526.1:n.405+75A>T
NM_207352.4:c.801+75A>T MANE Select	NP_997235.3:n.801+75A>T