Canonical Allele Identifier: CA112136717
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs1027631785

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210646A>G , CM000666.2:g.186210646A>G GRCh38
NC_000004.11:g.187131800A>G , CM000666.1:g.187131800A>G GRCh37
NC_000004.10:g.187368794A>G NCBI36
NG_007965.1:g.24127A>G
NG_012095.2:g.6668A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*5A>G (CYP4V2) MANE Select ENSP00000368079.4:n.*5A>G
ENST00000378802.4:c.*5A>G (CYP4V2) ENSP00000368079.4:n.*5A>G
ENST00000502665.1:n.818A>G (CYP4V2)
ENST00000507209.5:n.6281A>G (CYP4V2)
ENST00000511608.5:c.201+1374A>G (KLKB1)
ENST00000513354.5:n.673A>G (CYP4V2)
NM_207352.3:c.*5A>G (CYP4V2) NP_997235.3:n.*5A>G
XM_005262935.2:c.*5A>G (CYP4V2) XP_005262992.1:n.*5A>G
XM_006714184.2:c.*5A>G (CYP4V2) XP_006714247.1:n.*5A>G
XM_005262935.4:c.*5A>G (CYP4V2) XP_005262992.1:n.*5A>G
XM_017008037.1:c.*5A>G (CYP4V2) XP_016863526.1:n.*5A>G
NM_207352.4:c.*5A>G (CYP4V2) MANE Select NP_997235.3:n.*5A>G