Canonical Allele Identifier: CA358946727
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186192011-C-A
MyVariant Identifiers: chr4:g.187113165C>A (hg19) chr4:g.186192011C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186192011C>A , CM000666.2:g.186192011C>A GRCh38
NC_000004.11:g.187113165C>A , CM000666.1:g.187113165C>A GRCh37
NC_000004.10:g.187350159C>A NCBI36
NG_007965.1:g.5492C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.188C>A MANE Select ENSP00000368079.4:p.Ala63Glu
ENST00000378802.4:c.188C>A ENSP00000368079.4:p.Ala63Glu
NM_207352.3:c.188C>A NP_997235.3:p.Ala63Glu
XM_005262935.2:c.188C>A XP_005262992.1:p.Ala63Glu
XM_005262935.4:c.188C>A XP_005262992.1:p.Ala63Glu
XM_017008037.1:c.-123C>A XP_016863526.1:n.-123C>A
NM_207352.4:c.188C>A MANE Select NP_997235.3:p.Ala63Glu
Search 100 bp 5'
Search 100 bp 3'