Canonical Allele Identifier: CA2672896872
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205191_186205206del , CM000666.2:g.186205191_186205206del GRCh38
NC_000004.11:g.187126345_187126360del , CM000666.1:g.187126345_187126360del GRCh37
NC_000004.10:g.187363339_187363354del NCBI36
NG_007965.1:g.18672_18687del
NG_012095.2:g.1213_1228del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-9_994del
ENST00000378802.4:c.988-9_994del
ENST00000502665.1:n.223-9_229del
ENST00000507209.5:n.5677_5692del
ENST00000513354.5:n.78-9_84del
NM_207352.3:c.988-9_994del
XM_005262935.2:c.988-9_994del
XM_006714184.2:c.592-9_598del
XM_005262935.4:c.988-9_994del
XM_017008037.1:c.592-9_598del
NM_207352.4:c.988-9_994del