Canonical Allele Identifier: CA2672897720
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197590_186197615del , CM000666.2:g.186197590_186197615del GRCh38
NC_000004.11:g.187118744_187118769del , CM000666.1:g.187118744_187118769del GRCh37
NC_000004.10:g.187355738_187355763del NCBI36
NG_007965.1:g.11071_11096del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.662_674+13del
ENST00000378802.4:c.662_674+13del
ENST00000507209.5:n.1503_1515+13del
NM_207352.3:c.662_674+13del
XM_005262935.2:c.662_674+13del
XM_006714184.2:c.266_278+13del
XM_005262935.4:c.662_674+13del
XM_017008037.1:c.266_278+13del
NM_207352.4:c.662_674+13del