Canonical Allele Identifier: CA442882864
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187130389C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209235C>G , CM000666.2:g.186209235C>G GRCh38
NC_000004.11:g.187130389C>G , CM000666.1:g.187130389C>G GRCh37
NC_000004.10:g.187367383C>G NCBI36
NG_007965.1:g.22716C>G
NG_012095.2:g.5257C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1368C>G (CYP4V2) MANE Select ENSP00000368079.4:p.Ala456=
ENST00000378802.4:c.1368C>G (CYP4V2) ENSP00000368079.4:p.Ala456=
ENST00000502665.1:n.603C>G (CYP4V2)
ENST00000507209.5:n.6066C>G (CYP4V2)
ENST00000511608.5:c.164C>G (KLKB1)
ENST00000513354.5:n.458C>G (CYP4V2)
NM_207352.3:c.1368C>G (CYP4V2) NP_997235.3:p.Ala456=
XM_005262935.2:c.1365C>G (CYP4V2) XP_005262992.1:p.Ala455=
XM_006714184.2:c.972C>G (CYP4V2) XP_006714247.1:p.Ala324=
XM_005262935.4:c.1365C>G (CYP4V2) XP_005262992.1:p.Ala455=
XM_017008037.1:c.972C>G (CYP4V2) XP_016863526.1:p.Ala324=
NM_207352.4:c.1368C>G (CYP4V2) MANE Select NP_997235.3:p.Ala456=