Canonical Allele Identifier: CA358949206
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1341197524

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.994G>A MANE Select ENSP00000368079.4:p.Asp332Asn
ENST00000378802.4:c.994G>A ENSP00000368079.4:p.Asp332Asn
ENST00000502665.1:n.229G>A
ENST00000507209.5:n.5692G>A
ENST00000513354.5:n.84G>A
NM_207352.3:c.994G>A NP_997235.3:p.Asp332Asn
XM_005262935.2:c.994G>A XP_005262992.1:p.Asp332Asn
XM_006714184.2:c.598G>A XP_006714247.1:p.Asp200Asn
XM_005262935.4:c.994G>A XP_005262992.1:p.Asp332Asn
XM_017008037.1:c.598G>A XP_016863526.1:p.Asp200Asn
NM_207352.4:c.994G>A MANE Select NP_997235.3:p.Asp332Asn