Canonical Allele Identifier: CA3162902
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs766523003

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210649A>G , CM000666.2:g.186210649A>G GRCh38
NC_000004.11:g.187131803A>G , CM000666.1:g.187131803A>G GRCh37
NC_000004.10:g.187368797A>G NCBI36
NG_007965.1:g.24130A>G
NG_012095.2:g.6671A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*8A>G (CYP4V2) MANE Select ENSP00000368079.4:n.*8A>G
ENST00000378802.4:c.*8A>G (CYP4V2) ENSP00000368079.4:n.*8A>G
ENST00000502665.1:n.821A>G (CYP4V2)
ENST00000507209.5:n.6284A>G (CYP4V2)
ENST00000511608.5:c.201+1377A>G (KLKB1)
ENST00000513354.5:n.676A>G (CYP4V2)
NM_207352.3:c.*8A>G (CYP4V2) NP_997235.3:n.*8A>G
XM_005262935.2:c.*8A>G (CYP4V2) XP_005262992.1:n.*8A>G
XM_006714184.2:c.*8A>G (CYP4V2) XP_006714247.1:n.*8A>G
XM_005262935.4:c.*8A>G (CYP4V2) XP_005262992.1:n.*8A>G
XM_017008037.1:c.*8A>G (CYP4V2) XP_016863526.1:n.*8A>G
NM_207352.4:c.*8A>G (CYP4V2) MANE Select NP_997235.3:n.*8A>G