Canonical Allele Identifier: CA1519910607
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191812C= , CM000666.2:g.186191812C= GRCh38
NC_000004.11:g.187112966C= , CM000666.1:g.187112966C= GRCh37
NC_000004.10:g.187349960C= NCBI36
NG_007965.1:g.5293C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-12C= MANE Select ENSP00000368079.4:n.-12C=
ENST00000378802.4:c.-12C= ENSP00000368079.4:n.-12C=
NM_207352.3:c.-12C= NP_997235.3:n.-12C=
XM_005262935.2:c.-12C= XP_005262992.1:n.-12C=
XM_005262935.4:c.-12C= XP_005262992.1:n.-12C=
XM_017008037.1:c.-322C= XP_016863526.1:n.-322C=
NM_207352.4:c.-12C= MANE Select NP_997235.3:n.-12C=
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