Canonical Allele Identifier: CA149664
Gene: CYP4V2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 39267
dbSNP Id: rs1055138

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191887C>G , CM000666.2:g.186191887C>G GRCh38
NC_000004.11:g.187113041C>G , CM000666.1:g.187113041C>G GRCh37
NC_000004.10:g.187350035C>G NCBI36
NG_007965.1:g.5368C>G

Transcript Alleles

HGVS Amino-acid change
NM_207352.3:c.64C>G VV NP_997235.3:p.Leu22Val
XM_005262935.2:c.64C>G XP_005262992.1:p.Leu22Val
XM_005262935.4:c.64C>G XP_005262992.1:p.Leu22Val
XM_017008037.1:c.-247C>G XP_016863526.1:p.=
NM_207352.4:c.64C>G VV MANE Preferred NP_997235.3:p.Leu22Val
ENST00000378802.4:c.64C>G ENSP00000368079.4:p.Leu22Val