Canonical Allele Identifier: CA1519910332
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191710A= , CM000666.2:g.186191710A= GRCh38
NC_000004.11:g.187112864A= , CM000666.1:g.187112864A= GRCh37
NC_000004.10:g.187349858A= NCBI36
NG_007965.1:g.5191A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-114A= MANE Select ENSP00000368079.4:n.-114A=
ENST00000378802.4:c.-114A= ENSP00000368079.4:n.-114A=
NM_207352.3:c.-114A= NP_997235.3:n.-114A=
XM_005262935.2:c.-114A= XP_005262992.1:n.-114A=
XM_017008037.1:c.-424A= XP_016863526.1:n.-424A=
NM_207352.4:c.-114A= MANE Select NP_997235.3:n.-114A=