Canonical Allele Identifier: CA1519919154
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1736182826
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197412_186197414del , CM000666.2:g.186197412_186197414del GRCh38
NC_000004.11:g.187118566_187118568del , CM000666.1:g.187118566_187118568del GRCh37
NC_000004.10:g.187355560_187355562del NCBI36
NG_007965.1:g.10893_10895del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-121_605-119del MANE Select ENSP00000368079.4:n.605-121_605-119del
ENST00000378802.4:c.605-121_605-119del ENSP00000368079.4:n.605-121_605-119del
ENST00000507209.5:n.1325_1327del
NM_207352.3:c.605-121_605-119del NP_997235.3:n.605-121_605-119del
XM_005262935.2:c.605-121_605-119del XP_005262992.1:n.605-121_605-119del
XM_006714184.2:c.209-121_209-119del XP_006714247.1:n.209-121_209-119del
XM_005262935.4:c.605-121_605-119del XP_005262992.1:n.605-121_605-119del
XM_017008037.1:c.209-121_209-119del XP_016863526.1:n.209-121_209-119del
NM_207352.4:c.605-121_605-119del MANE Select NP_997235.3:n.605-121_605-119del
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