Canonical Allele Identifier: CA10620664
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 348322
dbSNP Id: rs886059284

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186211300A>G , CM000666.2:g.186211300A>G GRCh38
NC_000004.11:g.187132454A>G , CM000666.1:g.187132454A>G GRCh37
NC_000004.10:g.187369448A>G NCBI36
NG_007965.1:g.24781A>G
NG_012095.2:g.7322A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*659A>G (CYP4V2) MANE Select ENSP00000368079.4:n.*659A>G
ENST00000502665.1:n.1472A>G (CYP4V2)
ENST00000507209.5:n.6935A>G (CYP4V2)
ENST00000511608.5:c.201+2028A>G (KLKB1)
NM_207352.3:c.*659A>G (CYP4V2) NP_997235.3:n.*659A>G
XM_005262935.2:c.*659A>G (CYP4V2) XP_005262992.1:n.*659A>G
XM_006714184.2:c.*659A>G (CYP4V2) XP_006714247.1:n.*659A>G
XM_011531931.1:c.-3409A>G (KLKB1) XP_011530233.1:n.-3409A>G
XM_011531932.1:c.-3659A>G (KLKB1) XP_011530234.1:n.-3659A>G
XM_011531933.1:c.-3473A>G (KLKB1) XP_011530235.1:n.-3473A>G
XM_005262935.4:c.*659A>G (CYP4V2) XP_005262992.1:n.*659A>G
XM_017008037.1:c.*659A>G (CYP4V2) XP_016863526.1:n.*659A>G
NM_207352.4:c.*659A>G (CYP4V2) MANE Select NP_997235.3:n.*659A>G