Canonical Allele Identifier: CA358950382
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209113G>C , CM000666.2:g.186209113G>C GRCh38
NC_000004.11:g.187130267G>C , CM000666.1:g.187130267G>C GRCh37
NC_000004.10:g.187367261G>C NCBI36
NG_007965.1:g.22594G>C
NG_012095.2:g.5135G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1246G>C (CYP4V2) MANE Select ENSP00000368079.4:p.Gly416Arg
ENST00000378802.4:c.1246G>C (CYP4V2) ENSP00000368079.4:p.Gly416Arg
ENST00000502665.1:n.481G>C (CYP4V2)
ENST00000507209.5:n.5944G>C (CYP4V2)
ENST00000511608.5:c.42G>C (KLKB1)
ENST00000513354.5:n.336G>C (CYP4V2)
NM_207352.3:c.1246G>C (CYP4V2) NP_997235.3:p.Gly416Arg
XM_005262935.2:c.1243G>C (CYP4V2) XP_005262992.1:p.Gly415Arg
XM_006714184.2:c.850G>C (CYP4V2) XP_006714247.1:p.Gly284Arg
XM_005262935.4:c.1243G>C (CYP4V2) XP_005262992.1:p.Gly415Arg
XM_017008037.1:c.850G>C (CYP4V2) XP_016863526.1:p.Gly284Arg
NM_207352.4:c.1246G>C (CYP4V2) MANE Select NP_997235.3:p.Gly416Arg