Canonical Allele Identifier: CA358947799
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197580G>C , CM000666.2:g.186197580G>C GRCh38
NC_000004.11:g.187118734G>C , CM000666.1:g.187118734G>C GRCh37
NC_000004.10:g.187355728G>C NCBI36
NG_007965.1:g.11061G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.652G>C MANE Select ENSP00000368079.4:p.Glu218Gln
ENST00000378802.4:c.652G>C ENSP00000368079.4:p.Glu218Gln
ENST00000507209.5:n.1493G>C
NM_207352.3:c.652G>C NP_997235.3:p.Glu218Gln
XM_005262935.2:c.652G>C XP_005262992.1:p.Glu218Gln
XM_006714184.2:c.256G>C XP_006714247.1:p.Glu86Gln
XM_005262935.4:c.652G>C XP_005262992.1:p.Glu218Gln
XM_017008037.1:c.256G>C XP_016863526.1:p.Glu86Gln
NM_207352.4:c.652G>C MANE Select NP_997235.3:p.Glu218Gln