Canonical Allele Identifier: CA358946719
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186192007C>T , CM000666.2:g.186192007C>T GRCh38
NC_000004.11:g.187113161C>T , CM000666.1:g.187113161C>T GRCh37
NC_000004.10:g.187350155C>T NCBI36
NG_007965.1:g.5488C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.184C>T MANE Select ENSP00000368079.4:p.His62Tyr
ENST00000378802.4:c.184C>T ENSP00000368079.4:p.His62Tyr
NM_207352.3:c.184C>T NP_997235.3:p.His62Tyr
XM_005262935.2:c.184C>T XP_005262992.1:p.His62Tyr
XM_005262935.4:c.184C>T XP_005262992.1:p.His62Tyr
XM_017008037.1:c.-127C>T XP_016863526.1:n.-127C>T
NM_207352.4:c.184C>T MANE Select NP_997235.3:p.His62Tyr