Canonical Allele Identifier: CA2672898171
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199084_186199085dup , CM000666.2:g.186199084_186199085dup GRCh38
NC_000004.11:g.187120238_187120239dup , CM000666.1:g.187120238_187120239dup GRCh37
NC_000004.10:g.187357232_187357233dup NCBI36
NG_007965.1:g.12565_12566dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+1_801+2dup
ENST00000378802.4:c.801+1_801+2dup
ENST00000507209.5:n.1642+1_1642+2dup
NM_207352.3:c.801+1_801+2dup
XM_005262935.2:c.801+1_801+2dup
XM_006714184.2:c.405+1_405+2dup
XM_005262935.4:c.801+1_801+2dup
XM_017008037.1:c.405+1_405+2dup
NM_207352.4:c.801+1_801+2dup