Canonical Allele Identifier: CA1519889484

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736475381

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205678C>G , CM000666.2:g.186205678C>G	GRCh38
NC_000004.11:g.187126832C>G , CM000666.1:g.187126832C>G	GRCh37
NC_000004.10:g.187363826C>G	NCBI36
NG_007965.1:g.19159C>G
NG_012095.2:g.1700C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+376C>G MANE Select	ENSP00000368079.4:n.1090+376C>G
ENST00000378802.4:c.1090+376C>G	ENSP00000368079.4:n.1090+376C>G
ENST00000502665.1:n.325+376C>G
ENST00000507209.5:n.5788+376C>G
ENST00000513354.5:n.180+376C>G
NM_207352.3:c.1090+376C>G	NP_997235.3:n.1090+376C>G
XM_005262935.2:c.1090+376C>G	XP_005262992.1:n.1090+376C>G
XM_006714184.2:c.694+376C>G	XP_006714247.1:n.694+376C>G
XM_005262935.4:c.1090+376C>G	XP_005262992.1:n.1090+376C>G
XM_017008037.1:c.694+376C>G	XP_016863526.1:n.694+376C>G
NM_207352.4:c.1090+376C>G MANE Select	NP_997235.3:n.1090+376C>G