Canonical Allele Identifier: CA358949208

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1341197524
• MyVariant Identifiers: chr4:g.187126360G>C (hg19) ; chr4:g.186205206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205206G>C , CM000666.2:g.186205206G>C	GRCh38
NC_000004.11:g.187126360G>C , CM000666.1:g.187126360G>C	GRCh37
NC_000004.10:g.187363354G>C	NCBI36
NG_007965.1:g.18687G>C
NG_012095.2:g.1228G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.994G>C MANE Select	ENSP00000368079.4:p.Asp332His
ENST00000378802.4:c.994G>C	ENSP00000368079.4:p.Asp332His
ENST00000502665.1:n.229G>C
ENST00000507209.5:n.5692G>C
ENST00000513354.5:n.84G>C
NM_207352.3:c.994G>C	NP_997235.3:p.Asp332His
XM_005262935.2:c.994G>C	XP_005262992.1:p.Asp332His
XM_006714184.2:c.598G>C	XP_006714247.1:p.Asp200His
XM_005262935.4:c.994G>C	XP_005262992.1:p.Asp332His
XM_017008037.1:c.598G>C	XP_016863526.1:p.Asp200His
NM_207352.4:c.994G>C MANE Select	NP_997235.3:p.Asp332His