Canonical Allele Identifier: CA3162889

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs547395930
• ExAC: 4:187131751 G / A
• gnomAD v2: 4-187131751-G-A
• gnomAD v3: 4-186210597-G-A
• gnomAD v4: 4-186210597-G-A
• MyVariant Identifiers: chr4:g.187131751G>A (hg19) ; chr4:g.186210597G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210597G>A , CM000666.2:g.186210597G>A	GRCh38
NC_000004.11:g.187131751G>A , CM000666.1:g.187131751G>A	GRCh37
NC_000004.10:g.187368745G>A	NCBI36
NG_007965.1:g.24078G>A
NG_012095.2:g.6619G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1534G>A (CYP4V2) MANE Select	ENSP00000368079.4:p.Gly512Ser
ENST00000378802.4:c.1534G>A (CYP4V2)	ENSP00000368079.4:p.Gly512Ser
ENST00000502665.1:n.769G>A (CYP4V2)
ENST00000507209.5:n.6232G>A (CYP4V2)
ENST00000511608.5:c.201+1325G>A (KLKB1)
ENST00000513354.5:n.624G>A (CYP4V2)
NM_207352.3:c.1534G>A (CYP4V2)	NP_997235.3:p.Gly512Ser
XM_005262935.2:c.1531G>A (CYP4V2)	XP_005262992.1:p.Gly511Ser
XM_006714184.2:c.1138G>A (CYP4V2)	XP_006714247.1:p.Gly380Ser
XM_005262935.4:c.1531G>A (CYP4V2)	XP_005262992.1:p.Gly511Ser
XM_017008037.1:c.1138G>A (CYP4V2)	XP_016863526.1:p.Gly380Ser
NM_207352.4:c.1534G>A (CYP4V2) MANE Select	NP_997235.3:p.Gly512Ser