Canonical Allele Identifier: CA358948107
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199060A>G , CM000666.2:g.186199060A>G GRCh38
NC_000004.11:g.187120214A>G , CM000666.1:g.187120214A>G GRCh37
NC_000004.10:g.187357208A>G NCBI36
NG_007965.1:g.12541A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.778A>G MANE Select ENSP00000368079.4:p.Ile260Val
ENST00000378802.4:c.778A>G ENSP00000368079.4:p.Ile260Val
ENST00000507209.5:n.1619A>G
NM_207352.3:c.778A>G NP_997235.3:p.Ile260Val
XM_005262935.2:c.778A>G XP_005262992.1:p.Ile260Val
XM_006714184.2:c.382A>G XP_006714247.1:p.Ile128Val
XM_005262935.4:c.778A>G XP_005262992.1:p.Ile260Val
XM_017008037.1:c.382A>G XP_016863526.1:p.Ile128Val
NM_207352.4:c.778A>G MANE Select NP_997235.3:p.Ile260Val