Canonical Allele Identifier: CA1519914615
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194253C= , CM000666.2:g.186194253C= GRCh38
NC_000004.11:g.187115407C= , CM000666.1:g.187115407C= GRCh37
NC_000004.10:g.187352401C= NCBI36
NG_007965.1:g.7734C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-247C= MANE Select ENSP00000368079.4:n.215-247C=
ENST00000378802.4:c.215-247C= ENSP00000368079.4:n.215-247C=
NM_207352.3:c.215-247C= NP_997235.3:n.215-247C=
XM_005262935.2:c.215-247C= XP_005262992.1:n.215-247C=
XM_005262935.4:c.215-247C= XP_005262992.1:n.215-247C=
XM_017008037.1:c.-96-247C= XP_016863526.1:n.-96-247C=
NM_207352.4:c.215-247C= MANE Select NP_997235.3:n.215-247C=
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