Canonical Allele Identifier: CA1519888798

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1579972384

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205060T>G , CM000666.2:g.186205060T>G	GRCh38
NC_000004.11:g.187126214T>G , CM000666.1:g.187126214T>G	GRCh37
NC_000004.10:g.187363208T>G	NCBI36
NG_007965.1:g.18541T>G
NG_012095.2:g.1082T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-140T>G MANE Select	ENSP00000368079.4:n.988-140T>G
ENST00000378802.4:c.988-140T>G	ENSP00000368079.4:n.988-140T>G
ENST00000502665.1:n.222+2T>G
ENST00000507209.5:n.5546T>G
ENST00000513354.5:n.78-140T>G
NM_207352.3:c.988-140T>G	NP_997235.3:n.988-140T>G
XM_005262935.2:c.988-140T>G	XP_005262992.1:n.988-140T>G
XM_006714184.2:c.592-140T>G	XP_006714247.1:n.592-140T>G
XM_005262935.4:c.988-140T>G	XP_005262992.1:n.988-140T>G
XM_017008037.1:c.592-140T>G	XP_016863526.1:n.592-140T>G
NM_207352.4:c.988-140T>G MANE Select	NP_997235.3:n.988-140T>G