Canonical Allele Identifier: CA3162617
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348305
dbSNP Id: rs745471184

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197589C>T , CM000666.2:g.186197589C>T GRCh38
NC_000004.11:g.187118743C>T , CM000666.1:g.187118743C>T GRCh37
NC_000004.10:g.187355737C>T NCBI36
NG_007965.1:g.11070C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.661C>T MANE Select ENSP00000368079.4:p.Arg221Cys
ENST00000378802.4:c.661C>T ENSP00000368079.4:p.Arg221Cys
ENST00000507209.5:n.1502C>T
NM_207352.3:c.661C>T NP_997235.3:p.Arg221Cys
XM_005262935.2:c.661C>T XP_005262992.1:p.Arg221Cys
XM_006714184.2:c.265C>T XP_006714247.1:p.Arg89Cys
XM_005262935.4:c.661C>T XP_005262992.1:p.Arg221Cys
XM_017008037.1:c.265C>T XP_016863526.1:p.Arg89Cys
NM_207352.4:c.661C>T MANE Select NP_997235.3:p.Arg221Cys