Canonical Allele Identifier: CA1519915308
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194641G= , CM000666.2:g.186194641G= GRCh38
NC_000004.11:g.187115795G= , CM000666.1:g.187115795G= GRCh37
NC_000004.10:g.187352789G= NCBI36
NG_007965.1:g.8122G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.327+29G= MANE Select ENSP00000368079.4:n.327+29G=
ENST00000378802.4:c.327+29G= ENSP00000368079.4:n.327+29G=
NM_207352.3:c.327+29G= NP_997235.3:n.327+29G=
XM_005262935.2:c.327+29G= XP_005262992.1:n.327+29G=
XM_006714184.2:c.17+29G= XP_006714247.1:n.17+29G=
XM_005262935.4:c.327+29G= XP_005262992.1:n.327+29G=
XM_017008037.1:c.17+29G= XP_016863526.1:n.17+29G=
NM_207352.4:c.327+29G= MANE Select NP_997235.3:n.327+29G=