Canonical Allele Identifier: CA1519916833
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186195839C= , CM000666.2:g.186195839C= GRCh38
NC_000004.11:g.187116993C= , CM000666.1:g.187116993C= GRCh37
NC_000004.10:g.187353987C= NCBI36
NG_007965.1:g.9320C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.328-164C= MANE Select ENSP00000368079.4:n.328-164C=
ENST00000378802.4:c.328-164C= ENSP00000368079.4:n.328-164C=
NM_207352.3:c.328-164C= NP_997235.3:n.328-164C=
XM_005262935.2:c.328-164C= XP_005262992.1:n.328-164C=
XM_006714184.2:c.18-1101C= XP_006714247.1:n.18-1101C=
XM_005262935.4:c.328-164C= XP_005262992.1:n.328-164C=
XM_017008037.1:c.18-1101C= XP_016863526.1:n.18-1101C=
NM_207352.4:c.328-164C= MANE Select NP_997235.3:n.328-164C=
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