Canonical Allele Identifier: CA442882378

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs1452776586
• gnomAD v2: 4-187130254-C-T
• gnomAD v4: 4-186209100-C-T
• MyVariant Identifiers: chr4:g.187130254C>T (hg19) ; chr4:g.186209100C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209100C>T , CM000666.2:g.186209100C>T	GRCh38
NC_000004.11:g.187130254C>T , CM000666.1:g.187130254C>T	GRCh37
NC_000004.10:g.187367248C>T	NCBI36
NG_007965.1:g.22581C>T
NG_012095.2:g.5122C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1233C>T (CYP4V2) MANE Select	ENSP00000368079.4:p.Tyr411=
ENST00000378802.4:c.1233C>T (CYP4V2)	ENSP00000368079.4:p.Tyr411=
ENST00000502665.1:n.468C>T (CYP4V2)
ENST00000507209.5:n.5931C>T (CYP4V2)
ENST00000511608.5:c.29C>T (KLKB1)
ENST00000513354.5:n.323C>T (CYP4V2)
NM_207352.3:c.1233C>T (CYP4V2)	NP_997235.3:p.Tyr411=
XM_005262935.2:c.1230C>T (CYP4V2)	XP_005262992.1:p.Tyr410=
XM_006714184.2:c.837C>T (CYP4V2)	XP_006714247.1:p.Tyr279=
XM_005262935.4:c.1230C>T (CYP4V2)	XP_005262992.1:p.Tyr410=
XM_017008037.1:c.837C>T (CYP4V2)	XP_016863526.1:p.Tyr279=
NM_207352.4:c.1233C>T (CYP4V2) MANE Select	NP_997235.3:p.Tyr411=