Canonical Allele Identifier: CA3162909

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs748900264
• ExAC: 4:187131843 A / T
• gnomAD v2: 4-187131843-A-T
• gnomAD v4: 4-186210689-A-T
• MyVariant Identifiers: chr4:g.187131843A>T (hg19) ; chr4:g.186210689A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210689A>T , CM000666.2:g.186210689A>T	GRCh38
NC_000004.11:g.187131843A>T , CM000666.1:g.187131843A>T	GRCh37
NC_000004.10:g.187368837A>T	NCBI36
NG_007965.1:g.24170A>T
NG_012095.2:g.6711A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*48A>T (CYP4V2) MANE Select	ENSP00000368079.4:n.*48A>T
ENST00000378802.4:c.*48A>T (CYP4V2)	ENSP00000368079.4:n.*48A>T
ENST00000502665.1:n.861A>T (CYP4V2)
ENST00000507209.5:n.6324A>T (CYP4V2)
ENST00000511608.5:c.201+1417A>T (KLKB1)
ENST00000513354.5:n.716A>T (CYP4V2)
NM_207352.3:c.*48A>T (CYP4V2)	NP_997235.3:n.*48A>T
XM_005262935.2:c.*48A>T (CYP4V2)	XP_005262992.1:n.*48A>T
XM_006714184.2:c.*48A>T (CYP4V2)	XP_006714247.1:n.*48A>T
XM_005262935.4:c.*48A>T (CYP4V2)	XP_005262992.1:n.*48A>T
XM_017008037.1:c.*48A>T (CYP4V2)	XP_016863526.1:n.*48A>T
NM_207352.4:c.*48A>T (CYP4V2) MANE Select	NP_997235.3:n.*48A>T