Canonical Allele Identifier: CA1519910312
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191703A= , CM000666.2:g.186191703A= GRCh38
NC_000004.11:g.187112857A= , CM000666.1:g.187112857A= GRCh37
NC_000004.10:g.187349851A= NCBI36
NG_007965.1:g.5184A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-121A= MANE Select ENSP00000368079.4:n.-121A=
ENST00000378802.4:c.-121A= ENSP00000368079.4:n.-121A=
NM_207352.3:c.-121A= NP_997235.3:n.-121A=
XM_005262935.2:c.-121A= XP_005262992.1:n.-121A=
XM_017008037.1:c.-431A= XP_016863526.1:n.-431A=
NM_207352.4:c.-121A= MANE Select NP_997235.3:n.-121A=