Canonical Allele Identifier: CA358949334
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205243T>G , CM000666.2:g.186205243T>G GRCh38
NC_000004.11:g.187126397T>G , CM000666.1:g.187126397T>G GRCh37
NC_000004.10:g.187363391T>G NCBI36
NG_007965.1:g.18724T>G
NG_012095.2:g.1265T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1031T>G MANE Select ENSP00000368079.4:p.Leu344Arg
ENST00000378802.4:c.1031T>G ENSP00000368079.4:p.Leu344Arg
ENST00000502665.1:n.266T>G
ENST00000507209.5:n.5729T>G
ENST00000513354.5:n.121T>G
NM_207352.3:c.1031T>G NP_997235.3:p.Leu344Arg
XM_005262935.2:c.1031T>G XP_005262992.1:p.Leu344Arg
XM_006714184.2:c.635T>G XP_006714247.1:p.Leu212Arg
XM_005262935.4:c.1031T>G XP_005262992.1:p.Leu344Arg
XM_017008037.1:c.635T>G XP_016863526.1:p.Leu212Arg
NM_207352.4:c.1031T>G MANE Select NP_997235.3:p.Leu344Arg