Canonical Allele Identifier: CA1519915346
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194652C= , CM000666.2:g.186194652C= GRCh38
NC_000004.11:g.187115806C= , CM000666.1:g.187115806C= GRCh37
NC_000004.10:g.187352800C= NCBI36
NG_007965.1:g.8133C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.327+40C= MANE Select ENSP00000368079.4:n.327+40C=
ENST00000378802.4:c.327+40C= ENSP00000368079.4:n.327+40C=
NM_207352.3:c.327+40C= NP_997235.3:n.327+40C=
XM_005262935.2:c.327+40C= XP_005262992.1:n.327+40C=
XM_006714184.2:c.17+40C= XP_006714247.1:n.17+40C=
XM_005262935.4:c.327+40C= XP_005262992.1:n.327+40C=
XM_017008037.1:c.17+40C= XP_016863526.1:n.17+40C=
NM_207352.4:c.327+40C= MANE Select NP_997235.3:n.327+40C=
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