Canonical Allele Identifier: CA1519919007
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197311G= , CM000666.2:g.186197311G= GRCh38
NC_000004.11:g.187118465G= , CM000666.1:g.187118465G= GRCh37
NC_000004.10:g.187355459G= NCBI36
NG_007965.1:g.10792G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.604+181G= MANE Select ENSP00000368079.4:n.604+181G=
ENST00000378802.4:c.604+181G= ENSP00000368079.4:n.604+181G=
ENST00000507209.5:n.1224G=
NM_207352.3:c.604+181G= NP_997235.3:n.604+181G=
XM_005262935.2:c.604+181G= XP_005262992.1:n.604+181G=
XM_006714184.2:c.208+181G= XP_006714247.1:n.208+181G=
XM_005262935.4:c.604+181G= XP_005262992.1:n.604+181G=
XM_017008037.1:c.208+181G= XP_016863526.1:n.208+181G=
NM_207352.4:c.604+181G= MANE Select NP_997235.3:n.604+181G=
Search 100 bp 5'
Search 100 bp 3'