Canonical Allele Identifier: CA358946321
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191828C>A , CM000666.2:g.186191828C>A GRCh38
NC_000004.11:g.187112982C>A , CM000666.1:g.187112982C>A GRCh37
NC_000004.10:g.187349976C>A NCBI36
NG_007965.1:g.5309C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.5C>A MANE Select ENSP00000368079.4:p.Ala2Glu
ENST00000378802.4:c.5C>A ENSP00000368079.4:p.Ala2Glu
NM_207352.3:c.5C>A NP_997235.3:p.Ala2Glu
XM_005262935.2:c.5C>A XP_005262992.1:p.Ala2Glu
XM_005262935.4:c.5C>A XP_005262992.1:p.Ala2Glu
XM_017008037.1:c.-306C>A XP_016863526.1:n.-306C>A
NM_207352.4:c.5C>A MANE Select NP_997235.3:p.Ala2Glu