Canonical Allele Identifier: CA1519891399
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs777804916

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209085C>G , CM000666.2:g.186209085C>G GRCh38
NC_000004.11:g.187130239C>G , CM000666.1:g.187130239C>G GRCh37
NC_000004.10:g.187367233C>G NCBI36
NG_007965.1:g.22566C>G
NG_012095.2:g.5107C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1226-8C>G (CYP4V2) MANE Select ENSP00000368079.4:n.1226-8C>G
ENST00000378802.4:c.1226-8C>G (CYP4V2) ENSP00000368079.4:n.1226-8C>G
ENST00000502665.1:n.461-8C>G (CYP4V2)
ENST00000507209.5:n.5924-8C>G (CYP4V2)
ENST00000511608.5:c.22-8C>G (KLKB1)
ENST00000513354.5:n.316-8C>G (CYP4V2)
NM_207352.3:c.1226-8C>G (CYP4V2) NP_997235.3:n.1226-8C>G
XM_005262935.2:c.1226-11C>G (CYP4V2) XP_005262992.1:n.1226-11C>G
XM_006714184.2:c.830-8C>G (CYP4V2) XP_006714247.1:n.830-8C>G
XM_005262935.4:c.1226-11C>G (CYP4V2) XP_005262992.1:n.1226-11C>G
XM_017008037.1:c.830-8C>G (CYP4V2) XP_016863526.1:n.830-8C>G
NM_207352.4:c.1226-8C>G (CYP4V2) MANE Select NP_997235.3:n.1226-8C>G