Canonical Allele Identifier: CA358946717
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186192007-C-A
MyVariant Identifiers: chr4:g.187113161C>A (hg19) chr4:g.186192007C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186192007C>A , CM000666.2:g.186192007C>A GRCh38
NC_000004.11:g.187113161C>A , CM000666.1:g.187113161C>A GRCh37
NC_000004.10:g.187350155C>A NCBI36
NG_007965.1:g.5488C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.184C>A MANE Select ENSP00000368079.4:p.His62Asn
ENST00000378802.4:c.184C>A ENSP00000368079.4:p.His62Asn
NM_207352.3:c.184C>A NP_997235.3:p.His62Asn
XM_005262935.2:c.184C>A XP_005262992.1:p.His62Asn
XM_005262935.4:c.184C>A XP_005262992.1:p.His62Asn
XM_017008037.1:c.-127C>A XP_016863526.1:n.-127C>A
NM_207352.4:c.184C>A MANE Select NP_997235.3:p.His62Asn
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