Canonical Allele Identifier: CA1519919176
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1736184310
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197438_186197448del , CM000666.2:g.186197438_186197448del GRCh38
NC_000004.11:g.187118592_187118602del , CM000666.1:g.187118592_187118602del GRCh37
NC_000004.10:g.187355586_187355596del NCBI36
NG_007965.1:g.10919_10929del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-95_605-85del MANE Select ENSP00000368079.4:n.605-95_605-85del
ENST00000378802.4:c.605-95_605-85del ENSP00000368079.4:n.605-95_605-85del
ENST00000507209.5:n.1351_1361del
NM_207352.3:c.605-95_605-85del NP_997235.3:n.605-95_605-85del
XM_005262935.2:c.605-95_605-85del XP_005262992.1:n.605-95_605-85del
XM_006714184.2:c.209-95_209-85del XP_006714247.1:n.209-95_209-85del
XM_005262935.4:c.605-95_605-85del XP_005262992.1:n.605-95_605-85del
XM_017008037.1:c.209-95_209-85del XP_016863526.1:n.209-95_209-85del
NM_207352.4:c.605-95_605-85del MANE Select NP_997235.3:n.605-95_605-85del
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