Canonical Allele Identifier: CA792328608

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs1207967774
• gnomAD v3: 4-186209276-T-C
• gnomAD v4: 4-186209276-T-C
• MyVariant Identifiers: chr4:g.187130430T>C (hg19) ; chr4:g.186209276T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209276T>C , CM000666.2:g.186209276T>C	GRCh38
NC_000004.11:g.187130430T>C , CM000666.1:g.187130430T>C	GRCh37
NC_000004.10:g.187367424T>C	NCBI36
NG_007965.1:g.22757T>C
NG_012095.2:g.5298T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1405+4T>C (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+4T>C
ENST00000378802.4:c.1405+4T>C (CYP4V2)	ENSP00000368079.4:n.1405+4T>C
ENST00000502665.1:n.640+4T>C (CYP4V2)
ENST00000507209.5:n.6103+4T>C (CYP4V2)
ENST00000511608.5:c.201+4T>C (KLKB1)
ENST00000513354.5:n.495+4T>C (CYP4V2)
NM_207352.3:c.1405+4T>C (CYP4V2)	NP_997235.3:n.1405+4T>C
XM_005262935.2:c.1402+4T>C (CYP4V2)	XP_005262992.1:n.1402+4T>C
XM_006714184.2:c.1009+4T>C (CYP4V2)	XP_006714247.1:n.1009+4T>C
XM_005262935.4:c.1402+4T>C (CYP4V2)	XP_005262992.1:n.1402+4T>C
XM_017008037.1:c.1009+4T>C (CYP4V2)	XP_016863526.1:n.1009+4T>C
NM_207352.4:c.1405+4T>C (CYP4V2) MANE Select	NP_997235.3:n.1405+4T>C