Canonical Allele Identifier: CA792321960
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 854856
ClinVar RCV Id: RCV001059989
dbSNP Id: rs1300138505

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186201151_186201165del , CM000666.2:g.186201151_186201165del GRCh38
NC_000004.11:g.187122305_187122319del , CM000666.1:g.187122305_187122319del GRCh37
NC_000004.10:g.187359299_187359313del NCBI36
NG_007965.1:g.14632_14646del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.802-6_810del
ENST00000378802.4:c.802-6_810del
ENST00000507209.5:n.1643-6_1651del
NM_207352.3:c.802-6_810del
XM_005262935.2:c.802-6_810del
XM_006714184.2:c.406-6_414del
XM_005262935.4:c.802-6_810del
XM_017008037.1:c.406-6_414del
NM_207352.4:c.802-6_810del