Canonical Allele Identifier: CA358950696
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209262G>T , CM000666.2:g.186209262G>T GRCh38
NC_000004.11:g.187130416G>T , CM000666.1:g.187130416G>T GRCh37
NC_000004.10:g.187367410G>T NCBI36
NG_007965.1:g.22743G>T
NG_012095.2:g.5284G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1395G>T MANE Select ENSP00000368079.4:p.Arg465Ser
ENST00000378802.4:c.1395G>T ENSP00000368079.4:p.Arg465Ser
ENST00000502665.1:n.630G>T
ENST00000507209.5:n.6093G>T
ENST00000511608.5:n.191G>T
ENST00000513354.5:n.485G>T
NM_207352.3:c.1395G>T NP_997235.3:p.Arg465Ser
XM_005262935.2:c.1392G>T XP_005262992.1:p.Arg464Ser
XM_006714184.2:c.999G>T XP_006714247.1:p.Arg333Ser
XM_005262935.4:c.1392G>T XP_005262992.1:p.Arg464Ser
XM_017008037.1:c.999G>T XP_016863526.1:p.Arg333Ser
NM_207352.4:c.1395G>T MANE Select NP_997235.3:p.Arg465Ser