Canonical Allele Identifier: CA358947485
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197050A>G , CM000666.2:g.186197050A>G GRCh38
NC_000004.11:g.187118204A>G , CM000666.1:g.187118204A>G GRCh37
NC_000004.10:g.187355198A>G NCBI36
NG_007965.1:g.10531A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.524A>G MANE Select ENSP00000368079.4:p.Lys175Arg
ENST00000378802.4:c.524A>G ENSP00000368079.4:p.Lys175Arg
ENST00000507209.5:n.963A>G
NM_207352.3:c.524A>G NP_997235.3:p.Lys175Arg
XM_005262935.2:c.524A>G XP_005262992.1:p.Lys175Arg
XM_006714184.2:c.128A>G XP_006714247.1:p.Lys43Arg
XM_005262935.4:c.524A>G XP_005262992.1:p.Lys175Arg
XM_017008037.1:c.128A>G XP_016863526.1:p.Lys43Arg
NM_207352.4:c.524A>G MANE Select NP_997235.3:p.Lys175Arg