Canonical Allele Identifier: CA358950504
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs1579976949

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209171A>C , CM000666.2:g.186209171A>C GRCh38
NC_000004.11:g.187130325A>C , CM000666.1:g.187130325A>C GRCh37
NC_000004.10:g.187367319A>C NCBI36
NG_007965.1:g.22652A>C
NG_012095.2:g.5193A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1304A>C (CYP4V2) MANE Select ENSP00000368079.4:p.Asn435Thr
ENST00000378802.4:c.1304A>C (CYP4V2) ENSP00000368079.4:p.Asn435Thr
ENST00000502665.1:n.539A>C (CYP4V2)
ENST00000507209.5:n.6002A>C (CYP4V2)
ENST00000511608.5:c.100A>C (KLKB1)
ENST00000513354.5:n.394A>C (CYP4V2)
NM_207352.3:c.1304A>C (CYP4V2) NP_997235.3:p.Asn435Thr
XM_005262935.2:c.1301A>C (CYP4V2) XP_005262992.1:p.Asn434Thr
XM_006714184.2:c.908A>C (CYP4V2) XP_006714247.1:p.Asn303Thr
XM_005262935.4:c.1301A>C (CYP4V2) XP_005262992.1:p.Asn434Thr
XM_017008037.1:c.908A>C (CYP4V2) XP_016863526.1:p.Asn303Thr
NM_207352.4:c.1304A>C (CYP4V2) MANE Select NP_997235.3:p.Asn435Thr