Canonical Allele Identifier: CA358946804
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115660T>A (hg19) chr4:g.186194506T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194506T>A , CM000666.2:g.186194506T>A GRCh38
NC_000004.11:g.187115660T>A , CM000666.1:g.187115660T>A GRCh37
NC_000004.10:g.187352654T>A NCBI36
NG_007965.1:g.7987T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.221T>A MANE Select ENSP00000368079.4:p.Phe74Tyr
ENST00000378802.4:c.221T>A ENSP00000368079.4:p.Phe74Tyr
NM_207352.3:c.221T>A NP_997235.3:p.Phe74Tyr
XM_005262935.2:c.221T>A XP_005262992.1:p.Phe74Tyr
XM_005262935.4:c.221T>A XP_005262992.1:p.Phe74Tyr
XM_017008037.1:c.-90T>A XP_016863526.1:n.-90T>A
NM_207352.4:c.221T>A MANE Select NP_997235.3:p.Phe74Tyr
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