Canonical Allele Identifier: CA1519919271
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197507G= , CM000666.2:g.186197507G= GRCh38
NC_000004.11:g.187118661G= , CM000666.1:g.187118661G= GRCh37
NC_000004.10:g.187355655G= NCBI36
NG_007965.1:g.10988G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-26G= MANE Select ENSP00000368079.4:n.605-26G=
ENST00000378802.4:c.605-26G= ENSP00000368079.4:n.605-26G=
ENST00000507209.5:n.1420G=
NM_207352.3:c.605-26G= NP_997235.3:n.605-26G=
XM_005262935.2:c.605-26G= XP_005262992.1:n.605-26G=
XM_006714184.2:c.209-26G= XP_006714247.1:n.209-26G=
XM_005262935.4:c.605-26G= XP_005262992.1:n.605-26G=
XM_017008037.1:c.209-26G= XP_016863526.1:n.209-26G=
NM_207352.4:c.605-26G= MANE Select NP_997235.3:n.605-26G=