Canonical Allele Identifier: CA358947970
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199003C>T , CM000666.2:g.186199003C>T GRCh38
NC_000004.11:g.187120157C>T , CM000666.1:g.187120157C>T GRCh37
NC_000004.10:g.187357151C>T NCBI36
NG_007965.1:g.12484C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.721C>T MANE Select ENSP00000368079.4:p.Leu241Phe
ENST00000378802.4:c.721C>T ENSP00000368079.4:p.Leu241Phe
ENST00000507209.5:n.1562C>T
NM_207352.3:c.721C>T NP_997235.3:p.Leu241Phe
XM_005262935.2:c.721C>T XP_005262992.1:p.Leu241Phe
XM_006714184.2:c.325C>T XP_006714247.1:p.Leu109Phe
XM_005262935.4:c.721C>T XP_005262992.1:p.Leu241Phe
XM_017008037.1:c.325C>T XP_016863526.1:p.Leu109Phe
NM_207352.4:c.721C>T MANE Select NP_997235.3:p.Leu241Phe