Canonical Allele Identifier: CA1519914899
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194478C= , CM000666.2:g.186194478C= GRCh38
NC_000004.11:g.187115632C= , CM000666.1:g.187115632C= GRCh37
NC_000004.10:g.187352626C= NCBI36
NG_007965.1:g.7959C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.215-22C= MANE Select ENSP00000368079.4:n.215-22C=
ENST00000378802.4:c.215-22C= ENSP00000368079.4:n.215-22C=
NM_207352.3:c.215-22C= NP_997235.3:n.215-22C=
XM_005262935.2:c.215-22C= XP_005262992.1:n.215-22C=
XM_005262935.4:c.215-22C= XP_005262992.1:n.215-22C=
XM_017008037.1:c.-96-22C= XP_016863526.1:n.-96-22C=
NM_207352.4:c.215-22C= MANE Select NP_997235.3:n.215-22C=