Canonical Allele Identifier: CA2534324786
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186195922T>A , CM000666.2:g.186195922T>A GRCh38
NC_000004.11:g.187117076T>A , CM000666.1:g.187117076T>A GRCh37
NC_000004.10:g.187354070T>A NCBI36
NG_007965.1:g.9403T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.328-81T>A MANE Select ENSP00000368079.4:n.328-81T>A
ENST00000378802.4:c.328-81T>A ENSP00000368079.4:n.328-81T>A
NM_207352.3:c.328-81T>A NP_997235.3:n.328-81T>A
XM_005262935.2:c.328-81T>A XP_005262992.1:n.328-81T>A
XM_006714184.2:c.18-1018T>A XP_006714247.1:n.18-1018T>A
XM_005262935.4:c.328-81T>A XP_005262992.1:n.328-81T>A
XM_017008037.1:c.18-1018T>A XP_016863526.1:n.18-1018T>A
NM_207352.4:c.328-81T>A MANE Select NP_997235.3:n.328-81T>A
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