Canonical Allele Identifier: CA112138865
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs542607316

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186212575G>A , CM000666.2:g.186212575G>A GRCh38
NC_000004.11:g.187133729G>A , CM000666.1:g.187133729G>A GRCh37
NC_000004.10:g.187370723G>A NCBI36
NG_007965.1:g.26056G>A
NG_012095.2:g.8597G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*1934G>A (CYP4V2) MANE Select ENSP00000368079.4:n.*1934G>A
ENST00000502665.1:n.2747G>A (CYP4V2)
ENST00000507209.5:n.8210G>A (CYP4V2)
ENST00000511608.5:c.201+3303G>A (KLKB1)
NM_207352.3:c.*1934G>A (CYP4V2) NP_997235.3:n.*1934G>A
XM_005262935.2:c.*1934G>A (CYP4V2) XP_005262992.1:n.*1934G>A
XM_006714184.2:c.*1934G>A (CYP4V2) XP_006714247.1:n.*1934G>A
XM_011531931.1:c.-2134G>A (KLKB1) XP_011530233.1:n.-2134G>A
XM_011531932.1:c.-2384G>A (KLKB1) XP_011530234.1:n.-2384G>A
XM_011531933.1:c.-2198G>A (KLKB1) XP_011530235.1:n.-2198G>A
XM_005262935.4:c.*1934G>A (CYP4V2) XP_005262992.1:n.*1934G>A
XM_017008037.1:c.*1934G>A (CYP4V2) XP_016863526.1:n.*1934G>A
NM_207352.4:c.*1934G>A (CYP4V2) MANE Select NP_997235.3:n.*1934G>A