Canonical Allele Identifier: CA1519920389
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198851C= , CM000666.2:g.186198851C= GRCh38
NC_000004.11:g.187120005C= , CM000666.1:g.187120005C= GRCh37
NC_000004.10:g.187356999C= NCBI36
NG_007965.1:g.12332C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.675-106C= MANE Select ENSP00000368079.4:n.675-106C=
ENST00000378802.4:c.675-106C= ENSP00000368079.4:n.675-106C=
ENST00000507209.5:n.1516-106C=
NM_207352.3:c.675-106C= NP_997235.3:n.675-106C=
XM_005262935.2:c.675-106C= XP_005262992.1:n.675-106C=
XM_006714184.2:c.279-106C= XP_006714247.1:n.279-106C=
XM_005262935.4:c.675-106C= XP_005262992.1:n.675-106C=
XM_017008037.1:c.279-106C= XP_016863526.1:n.279-106C=
NM_207352.4:c.675-106C= MANE Select NP_997235.3:n.675-106C=
Search 100 bp 5'
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