Canonical Allele Identifier: CA2672892283
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191817-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191821del , CM000666.2:g.186191821del GRCh38
NC_000004.11:g.187112975del , CM000666.1:g.187112975del GRCh37
NC_000004.10:g.187349969del NCBI36
NG_007965.1:g.5302del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-3del MANE Select ENSP00000368079.4:n.-3del
ENST00000378802.4:c.-3del ENSP00000368079.4:n.-3del
NM_207352.3:c.-3del NP_997235.3:n.-3del
XM_005262935.2:c.-3del XP_005262992.1:n.-3del
XM_005262935.4:c.-3del XP_005262992.1:n.-3del
XM_017008037.1:c.-313del XP_016863526.1:n.-313del
NM_207352.4:c.-3del MANE Select NP_997235.3:n.-3del
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