Canonical Allele Identifier: CA1519916972
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186195972T= , CM000666.2:g.186195972T= GRCh38
NC_000004.11:g.187117126T= , CM000666.1:g.187117126T= GRCh37
NC_000004.10:g.187354120T= NCBI36
NG_007965.1:g.9453T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.328-31T= MANE Select ENSP00000368079.4:n.328-31T=
ENST00000378802.4:c.328-31T= ENSP00000368079.4:n.328-31T=
NM_207352.3:c.328-31T= NP_997235.3:n.328-31T=
XM_005262935.2:c.328-31T= XP_005262992.1:n.328-31T=
XM_006714184.2:c.18-968T= XP_006714247.1:n.18-968T=
XM_005262935.4:c.328-31T= XP_005262992.1:n.328-31T=
XM_017008037.1:c.18-968T= XP_016863526.1:n.18-968T=
NM_207352.4:c.328-31T= MANE Select NP_997235.3:n.328-31T=
Search 100 bp 5'
Search 100 bp 3'