Canonical Allele Identifier: CA3162488
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424951
ClinVar RCV Id: RCV001924162
dbSNP Id: rs770301714

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194557A>G , CM000666.2:g.186194557A>G GRCh38
NC_000004.11:g.187115711A>G , CM000666.1:g.187115711A>G GRCh37
NC_000004.10:g.187352705A>G NCBI36
NG_007965.1:g.8038A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.272A>G MANE Select ENSP00000368079.4:p.Lys91Arg
ENST00000378802.4:c.272A>G ENSP00000368079.4:p.Lys91Arg
NM_207352.3:c.272A>G NP_997235.3:p.Lys91Arg
XM_005262935.2:c.272A>G XP_005262992.1:p.Lys91Arg
XM_006714184.2:c.-39A>G XP_006714247.1:n.-39A>G
XM_005262935.4:c.272A>G XP_005262992.1:p.Lys91Arg
XM_017008037.1:c.-39A>G XP_016863526.1:n.-39A>G
NM_207352.4:c.272A>G MANE Select NP_997235.3:p.Lys91Arg