Canonical Allele Identifier: CA2708145112
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs2126589046
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186200820del , CM000666.2:g.186200820del GRCh38
NC_000004.11:g.187121974del , CM000666.1:g.187121974del GRCh37
NC_000004.10:g.187358968del NCBI36
NG_007965.1:g.14301del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.802-337del MANE Select ENSP00000368079.4:n.802-337del
ENST00000378802.4:c.802-337del ENSP00000368079.4:n.802-337del
ENST00000507209.5:n.1643-337del
NM_207352.3:c.802-337del NP_997235.3:n.802-337del
XM_005262935.2:c.802-337del XP_005262992.1:n.802-337del
XM_006714184.2:c.406-337del XP_006714247.1:n.406-337del
XM_005262935.4:c.802-337del XP_005262992.1:n.802-337del
XM_017008037.1:c.406-337del XP_016863526.1:n.406-337del
NM_207352.4:c.802-337del MANE Select NP_997235.3:n.802-337del
Search 100 bp 5'
Search 100 bp 3'