Canonical Allele Identifier: CA792330102

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs1204954305
• gnomAD v4: 4-186211341-T-G
• MyVariant Identifiers: chr4:g.187132495T>G (hg19) ; chr4:g.186211341T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211341T>G , CM000666.2:g.186211341T>G	GRCh38
NC_000004.11:g.187132495T>G , CM000666.1:g.187132495T>G	GRCh37
NC_000004.10:g.187369489T>G	NCBI36
NG_007965.1:g.24822T>G
NG_012095.2:g.7363T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*700T>G (CYP4V2) MANE Select	ENSP00000368079.4:n.*700T>G
ENST00000502665.1:n.1513T>G (CYP4V2)
ENST00000507209.5:n.6976T>G (CYP4V2)
ENST00000511608.5:c.201+2069T>G (KLKB1)
NM_207352.3:c.*700T>G (CYP4V2)	NP_997235.3:n.*700T>G
XM_005262935.2:c.*700T>G (CYP4V2)	XP_005262992.1:n.*700T>G
XM_006714184.2:c.*700T>G (CYP4V2)	XP_006714247.1:n.*700T>G
XM_011531931.1:c.-3368T>G (KLKB1)	XP_011530233.1:n.-3368T>G
XM_011531932.1:c.-3618T>G (KLKB1)	XP_011530234.1:n.-3618T>G
XM_011531933.1:c.-3432T>G (KLKB1)	XP_011530235.1:n.-3432T>G
XM_005262935.4:c.*700T>G (CYP4V2)	XP_005262992.1:n.*700T>G
XM_017008037.1:c.*700T>G (CYP4V2)	XP_016863526.1:n.*700T>G
NM_207352.4:c.*700T>G (CYP4V2) MANE Select	NP_997235.3:n.*700T>G