Canonical Allele Identifier: CA1071975351
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs1301950747

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186211282C>T , CM000666.2:g.186211282C>T GRCh38
NC_000004.11:g.187132436C>T , CM000666.1:g.187132436C>T GRCh37
NC_000004.10:g.187369430C>T NCBI36
NG_007965.1:g.24763C>T
NG_012095.2:g.7304C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*641C>T (CYP4V2) MANE Select ENSP00000368079.4:n.*641C>T
ENST00000502665.1:n.1454C>T (CYP4V2)
ENST00000507209.5:n.6917C>T (CYP4V2)
ENST00000511608.5:c.201+2010C>T (KLKB1)
NM_207352.3:c.*641C>T (CYP4V2) NP_997235.3:n.*641C>T
XM_005262935.2:c.*641C>T (CYP4V2) XP_005262992.1:n.*641C>T
XM_006714184.2:c.*641C>T (CYP4V2) XP_006714247.1:n.*641C>T
XM_011531931.1:c.-3427C>T (KLKB1) XP_011530233.1:n.-3427C>T
XM_011531932.1:c.-3677C>T (KLKB1) XP_011530234.1:n.-3677C>T
XM_011531933.1:c.-3491C>T (KLKB1) XP_011530235.1:n.-3491C>T
XM_005262935.4:c.*641C>T (CYP4V2) XP_005262992.1:n.*641C>T
XM_017008037.1:c.*641C>T (CYP4V2) XP_016863526.1:n.*641C>T
NM_207352.4:c.*641C>T (CYP4V2) MANE Select NP_997235.3:n.*641C>T