Canonical Allele Identifier: CA1519910328
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191709G= , CM000666.2:g.186191709G= GRCh38
NC_000004.11:g.187112863G= , CM000666.1:g.187112863G= GRCh37
NC_000004.10:g.187349857G= NCBI36
NG_007965.1:g.5190G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-115G= MANE Select ENSP00000368079.4:n.-115G=
ENST00000378802.4:c.-115G= ENSP00000368079.4:n.-115G=
NM_207352.3:c.-115G= NP_997235.3:n.-115G=
XM_005262935.2:c.-115G= XP_005262992.1:n.-115G=
XM_017008037.1:c.-425G= XP_016863526.1:n.-425G=
NM_207352.4:c.-115G= MANE Select NP_997235.3:n.-115G=