Canonical Allele Identifier: CA2518272599
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191693-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191693G>A , CM000666.2:g.186191693G>A GRCh38
NC_000004.11:g.187112847G>A , CM000666.1:g.187112847G>A GRCh37
NC_000004.10:g.187349841G>A NCBI36
NG_007965.1:g.5174G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-131G>A MANE Select ENSP00000368079.4:n.-131G>A
ENST00000378802.4:c.-131G>A ENSP00000368079.4:n.-131G>A
NM_207352.3:c.-131G>A NP_997235.3:n.-131G>A
XM_005262935.2:c.-131G>A XP_005262992.1:n.-131G>A
XM_017008037.1:c.-441G>A XP_016863526.1:n.-441G>A
NM_207352.4:c.-131G>A MANE Select NP_997235.3:n.-131G>A
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