Canonical Allele Identifier: CA358946903

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1561430865
• gnomAD v3: 4-186194547-C-G
• gnomAD v4: 4-186194547-C-G
• MyVariant Identifiers: chr4:g.187115701C>G (hg19) ; chr4:g.186194547C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194547C>G , CM000666.2:g.186194547C>G	GRCh38
NC_000004.11:g.187115701C>G , CM000666.1:g.187115701C>G	GRCh37
NC_000004.10:g.187352695C>G	NCBI36
NG_007965.1:g.8028C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.262C>G MANE Select	ENSP00000368079.4:p.Pro88Ala
ENST00000378802.4:c.262C>G	ENSP00000368079.4:p.Pro88Ala
NM_207352.3:c.262C>G	NP_997235.3:p.Pro88Ala
XM_005262935.2:c.262C>G	XP_005262992.1:p.Pro88Ala
XM_006714184.2:c.-49C>G	XP_006714247.1:n.-49C>G
XM_005262935.4:c.262C>G	XP_005262992.1:p.Pro88Ala
XM_017008037.1:c.-49C>G	XP_016863526.1:n.-49C>G
NM_207352.4:c.262C>G MANE Select	NP_997235.3:p.Pro88Ala