Canonical Allele Identifier: CA358950707
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209267G>A , CM000666.2:g.186209267G>A GRCh38
NC_000004.11:g.187130421G>A , CM000666.1:g.187130421G>A GRCh37
NC_000004.10:g.187367415G>A NCBI36
NG_007965.1:g.22748G>A
NG_012095.2:g.5289G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1400G>A MANE Select ENSP00000368079.4:p.Cys467Tyr
ENST00000378802.4:c.1400G>A ENSP00000368079.4:p.Cys467Tyr
ENST00000502665.1:n.635G>A
ENST00000507209.5:n.6098G>A
ENST00000511608.5:n.196G>A
ENST00000513354.5:n.490G>A
NM_207352.3:c.1400G>A NP_997235.3:p.Cys467Tyr
XM_005262935.2:c.1397G>A XP_005262992.1:p.Cys466Tyr
XM_006714184.2:c.1004G>A XP_006714247.1:p.Cys335Tyr
XM_005262935.4:c.1397G>A XP_005262992.1:p.Cys466Tyr
XM_017008037.1:c.1004G>A XP_016863526.1:p.Cys335Tyr
NM_207352.4:c.1400G>A MANE Select NP_997235.3:p.Cys467Tyr