Canonical Allele Identifier: CA358947906
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198977G>T , CM000666.2:g.186198977G>T GRCh38
NC_000004.11:g.187120131G>T , CM000666.1:g.187120131G>T GRCh37
NC_000004.10:g.187357125G>T NCBI36
NG_007965.1:g.12458G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.695G>T MANE Select ENSP00000368079.4:p.Arg232Leu
ENST00000378802.4:c.695G>T ENSP00000368079.4:p.Arg232Leu
ENST00000507209.5:n.1536G>T
NM_207352.3:c.695G>T NP_997235.3:p.Arg232Leu
XM_005262935.2:c.695G>T XP_005262992.1:p.Arg232Leu
XM_006714184.2:c.299G>T XP_006714247.1:p.Arg100Leu
XM_005262935.4:c.695G>T XP_005262992.1:p.Arg232Leu
XM_017008037.1:c.299G>T XP_016863526.1:p.Arg100Leu
NM_207352.4:c.695G>T MANE Select NP_997235.3:p.Arg232Leu