Canonical Allele Identifier: CA792321756
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1187870176
gnomAD v3: 4-186200665-GA-G
gnomAD v4: 4-186200665-GA-G
MyVariant Identifiers: chr4:g.187121820del (hg19) chr4:g.186200666del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186200666del , CM000666.2:g.186200666del GRCh38
NC_000004.11:g.187121820del , CM000666.1:g.187121820del GRCh37
NC_000004.10:g.187358814del NCBI36
NG_007965.1:g.14147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.802-491del MANE Select ENSP00000368079.4:n.802-491del
ENST00000378802.4:c.802-491del ENSP00000368079.4:n.802-491del
ENST00000507209.5:n.1643-491del
NM_207352.3:c.802-491del NP_997235.3:n.802-491del
XM_005262935.2:c.802-491del XP_005262992.1:n.802-491del
XM_006714184.2:c.406-491del XP_006714247.1:n.406-491del
XM_005262935.4:c.802-491del XP_005262992.1:n.802-491del
XM_017008037.1:c.406-491del XP_016863526.1:n.406-491del
NM_207352.4:c.802-491del MANE Select NP_997235.3:n.802-491del
Search 100 bp 5'
Search 100 bp 3'