Canonical Allele Identifier: CA358947877
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198964G>T , CM000666.2:g.186198964G>T GRCh38
NC_000004.11:g.187120118G>T , CM000666.1:g.187120118G>T GRCh37
NC_000004.10:g.187357112G>T NCBI36
NG_007965.1:g.12445G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.682G>T MANE Select ENSP00000368079.4:p.Glu228Ter
ENST00000378802.4:c.682G>T ENSP00000368079.4:p.Glu228Ter
ENST00000507209.5:n.1523G>T
NM_207352.3:c.682G>T NP_997235.3:p.Glu228Ter
XM_005262935.2:c.682G>T XP_005262992.1:p.Glu228Ter
XM_006714184.2:c.286G>T XP_006714247.1:p.Glu96Ter
XM_005262935.4:c.682G>T XP_005262992.1:p.Glu228Ter
XM_017008037.1:c.286G>T XP_016863526.1:p.Glu96Ter
NM_207352.4:c.682G>T MANE Select NP_997235.3:p.Glu228Ter