Canonical Allele Identifier: CA1519893638

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs1736760723

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186212577T>C , CM000666.2:g.186212577T>C	GRCh38
NC_000004.11:g.187133731T>C , CM000666.1:g.187133731T>C	GRCh37
NC_000004.10:g.187370725T>C	NCBI36
NG_007965.1:g.26058T>C
NG_012095.2:g.8599T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.*1936T>C (CYP4V2) MANE Select	ENSP00000368079.4:n.*1936T>C
ENST00000502665.1:n.2749T>C (CYP4V2)
ENST00000507209.5:n.8212T>C (CYP4V2)
ENST00000511608.5:c.201+3305T>C (KLKB1)
NM_207352.3:c.*1936T>C (CYP4V2)	NP_997235.3:n.*1936T>C
XM_005262935.2:c.*1936T>C (CYP4V2)	XP_005262992.1:n.*1936T>C
XM_006714184.2:c.*1936T>C (CYP4V2)	XP_006714247.1:n.*1936T>C
XM_011531931.1:c.-2132T>C (KLKB1)	XP_011530233.1:n.-2132T>C
XM_011531932.1:c.-2382T>C (KLKB1)	XP_011530234.1:n.-2382T>C
XM_011531933.1:c.-2196T>C (KLKB1)	XP_011530235.1:n.-2196T>C
XM_005262935.4:c.*1936T>C (CYP4V2)	XP_005262992.1:n.*1936T>C
XM_017008037.1:c.*1936T>C (CYP4V2)	XP_016863526.1:n.*1936T>C
NM_207352.4:c.*1936T>C (CYP4V2) MANE Select	NP_997235.3:n.*1936T>C