Canonical Allele Identifier: CA3162804
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs757183148

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209088G>A , CM000666.2:g.186209088G>A GRCh38
NC_000004.11:g.187130242G>A , CM000666.1:g.187130242G>A GRCh37
NC_000004.10:g.187367236G>A NCBI36
NG_007965.1:g.22569G>A
NG_012095.2:g.5110G>A

Transcript Alleles

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