Canonical Allele Identifier: CA1519888794
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205059G= , CM000666.2:g.186205059G= GRCh38
NC_000004.11:g.187126213G= , CM000666.1:g.187126213G= GRCh37
NC_000004.10:g.187363207G= NCBI36
NG_007965.1:g.18540G=
NG_012095.2:g.1081G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-141G= MANE Select ENSP00000368079.4:n.988-141G=
ENST00000378802.4:c.988-141G= ENSP00000368079.4:n.988-141G=
ENST00000502665.1:n.222+1G=
ENST00000507209.5:n.5545G=
ENST00000513354.5:n.78-141G=
NM_207352.3:c.988-141G= NP_997235.3:n.988-141G=
XM_005262935.2:c.988-141G= XP_005262992.1:n.988-141G=
XM_006714184.2:c.592-141G= XP_006714247.1:n.592-141G=
XM_005262935.4:c.988-141G= XP_005262992.1:n.988-141G=
XM_017008037.1:c.592-141G= XP_016863526.1:n.592-141G=
NM_207352.4:c.988-141G= MANE Select NP_997235.3:n.988-141G=