Canonical Allele Identifier: CA557395927

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs1360401666
• gnomAD v2: 4-187131592-C-G
• gnomAD v4: 4-186210438-C-G
• MyVariant Identifiers: chr4:g.187131592C>G (hg19) ; chr4:g.186210438C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210438C>G , CM000666.2:g.186210438C>G	GRCh38
NC_000004.11:g.187131592C>G , CM000666.1:g.187131592C>G	GRCh37
NC_000004.10:g.187368586C>G	NCBI36
NG_007965.1:g.23919C>G
NG_012095.2:g.6460C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1406-31C>G (CYP4V2) MANE Select	ENSP00000368079.4:n.1406-31C>G
ENST00000378802.4:c.1406-31C>G (CYP4V2)	ENSP00000368079.4:n.1406-31C>G
ENST00000502665.1:n.641-31C>G (CYP4V2)
ENST00000507209.5:n.6104-31C>G (CYP4V2)
ENST00000511608.5:c.201+1166C>G (KLKB1)
ENST00000513354.5:n.496-31C>G (CYP4V2)
NM_207352.3:c.1406-31C>G (CYP4V2)	NP_997235.3:n.1406-31C>G
XM_005262935.2:c.1403-31C>G (CYP4V2)	XP_005262992.1:n.1403-31C>G
XM_006714184.2:c.1010-31C>G (CYP4V2)	XP_006714247.1:n.1010-31C>G
XM_005262935.4:c.1403-31C>G (CYP4V2)	XP_005262992.1:n.1403-31C>G
XM_017008037.1:c.1010-31C>G (CYP4V2)	XP_016863526.1:n.1010-31C>G
NM_207352.4:c.1406-31C>G (CYP4V2) MANE Select	NP_997235.3:n.1406-31C>G