Canonical Allele Identifier: CA1519919042
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197341G= , CM000666.2:g.186197341G= GRCh38
NC_000004.11:g.187118495G= , CM000666.1:g.187118495G= GRCh37
NC_000004.10:g.187355489G= NCBI36
NG_007965.1:g.10822G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-192G= MANE Select ENSP00000368079.4:n.605-192G=
ENST00000378802.4:c.605-192G= ENSP00000368079.4:n.605-192G=
ENST00000507209.5:n.1254G=
NM_207352.3:c.605-192G= NP_997235.3:n.605-192G=
XM_005262935.2:c.605-192G= XP_005262992.1:n.605-192G=
XM_006714184.2:c.209-192G= XP_006714247.1:n.209-192G=
XM_005262935.4:c.605-192G= XP_005262992.1:n.605-192G=
XM_017008037.1:c.209-192G= XP_016863526.1:n.209-192G=
NM_207352.4:c.605-192G= MANE Select NP_997235.3:n.605-192G=
Search 100 bp 5'
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