Canonical Allele Identifier: CA1519915261
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194622T= , CM000666.2:g.186194622T= GRCh38
NC_000004.11:g.187115776T= , CM000666.1:g.187115776T= GRCh37
NC_000004.10:g.187352770T= NCBI36
NG_007965.1:g.8103T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.327+10T= MANE Select ENSP00000368079.4:n.327+10T=
ENST00000378802.4:c.327+10T= ENSP00000368079.4:n.327+10T=
NM_207352.3:c.327+10T= NP_997235.3:n.327+10T=
XM_005262935.2:c.327+10T= XP_005262992.1:n.327+10T=
XM_006714184.2:c.17+10T= XP_006714247.1:n.17+10T=
XM_005262935.4:c.327+10T= XP_005262992.1:n.327+10T=
XM_017008037.1:c.17+10T= XP_016863526.1:n.17+10T=
NM_207352.4:c.327+10T= MANE Select NP_997235.3:n.327+10T=