Canonical Allele Identifier: CA1519888552
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204824C= , CM000666.2:g.186204824C= GRCh38
NC_000004.11:g.187125978C= , CM000666.1:g.187125978C= GRCh37
NC_000004.10:g.187362972C= NCBI36
NG_007965.1:g.18305C=
NG_012095.2:g.846C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-376C= MANE Select ENSP00000368079.4:n.988-376C=
ENST00000378802.4:c.988-376C= ENSP00000368079.4:n.988-376C=
ENST00000507209.5:n.5310C=
ENST00000513354.5:n.77+367C=
NM_207352.3:c.988-376C= NP_997235.3:n.988-376C=
XM_005262935.2:c.988-376C= XP_005262992.1:n.988-376C=
XM_006714184.2:c.592-376C= XP_006714247.1:n.592-376C=
XM_005262935.4:c.988-376C= XP_005262992.1:n.988-376C=
XM_017008037.1:c.592-376C= XP_016863526.1:n.592-376C=
NM_207352.4:c.988-376C= MANE Select NP_997235.3:n.988-376C=
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