Canonical Allele Identifier: CA3162511
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs745684760
ExAC: 4:187115801 TG / T
gnomAD v2: 4-187115801-TG-T
gnomAD v3: 4-186194647-TG-T
gnomAD v4: 4-186194647-TG-T
MyVariant Identifiers: chr4:g.187115802del (hg19) chr4:g.186194648del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194648del , CM000666.2:g.186194648del GRCh38
NC_000004.11:g.187115802del , CM000666.1:g.187115802del GRCh37
NC_000004.10:g.187352796del NCBI36
NG_007965.1:g.8129del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.327+36del MANE Select ENSP00000368079.4:n.327+36del
ENST00000378802.4:c.327+36del ENSP00000368079.4:n.327+36del
NM_207352.3:c.327+36del NP_997235.3:n.327+36del
XM_005262935.2:c.327+36del XP_005262992.1:n.327+36del
XM_006714184.2:c.17+36del XP_006714247.1:n.17+36del
XM_005262935.4:c.327+36del XP_005262992.1:n.327+36del
XM_017008037.1:c.17+36del XP_016863526.1:n.17+36del
NM_207352.4:c.327+36del MANE Select NP_997235.3:n.327+36del
Search 100 bp 5'
Search 100 bp 3'