Canonical Allele Identifier: CA358947806
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197583T>G , CM000666.2:g.186197583T>G GRCh38
NC_000004.11:g.187118737T>G , CM000666.1:g.187118737T>G GRCh37
NC_000004.10:g.187355731T>G NCBI36
NG_007965.1:g.11064T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.655T>G MANE Select ENSP00000368079.4:p.Tyr219Asp
ENST00000378802.4:c.655T>G ENSP00000368079.4:p.Tyr219Asp
ENST00000507209.5:n.1496T>G
NM_207352.3:c.655T>G NP_997235.3:p.Tyr219Asp
XM_005262935.2:c.655T>G XP_005262992.1:p.Tyr219Asp
XM_006714184.2:c.259T>G XP_006714247.1:p.Tyr87Asp
XM_005262935.4:c.655T>G XP_005262992.1:p.Tyr219Asp
XM_017008037.1:c.259T>G XP_016863526.1:p.Tyr87Asp
NM_207352.4:c.655T>G MANE Select NP_997235.3:p.Tyr219Asp