Canonical Allele Identifier: CA1519910892
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191922G= , CM000666.2:g.186191922G= GRCh38
NC_000004.11:g.187113076G= , CM000666.1:g.187113076G= GRCh37
NC_000004.10:g.187350070G= NCBI36
NG_007965.1:g.5403G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.99G= MANE Select ENSP00000368079.4:p.Leu33=
ENST00000378802.4:c.99G= ENSP00000368079.4:p.Leu33=
NM_207352.3:c.99G= NP_997235.3:p.Leu33=
XM_005262935.2:c.99G= XP_005262992.1:p.Leu33=
XM_005262935.4:c.99G= XP_005262992.1:p.Leu33=
XM_017008037.1:c.-212G= XP_016863526.1:n.-212G=
NM_207352.4:c.99G= MANE Select NP_997235.3:p.Leu33=