Canonical Allele Identifier: CA1519910319
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191706G= , CM000666.2:g.186191706G= GRCh38
NC_000004.11:g.187112860G= , CM000666.1:g.187112860G= GRCh37
NC_000004.10:g.187349854G= NCBI36
NG_007965.1:g.5187G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-118G= MANE Select ENSP00000368079.4:n.-118G=
ENST00000378802.4:c.-118G= ENSP00000368079.4:n.-118G=
NM_207352.3:c.-118G= NP_997235.3:n.-118G=
XM_005262935.2:c.-118G= XP_005262992.1:n.-118G=
XM_017008037.1:c.-428G= XP_016863526.1:n.-428G=
NM_207352.4:c.-118G= MANE Select NP_997235.3:n.-118G=