Canonical Allele Identifier: CA358947029

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1441824959
• gnomAD v2: 4-187115765-A-G
• gnomAD v4: 4-186194611-A-G
• MyVariant Identifiers: chr4:g.187115765A>G (hg19) ; chr4:g.186194611A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194611A>G , CM000666.2:g.186194611A>G	GRCh38
NC_000004.11:g.187115765A>G , CM000666.1:g.187115765A>G	GRCh37
NC_000004.10:g.187352759A>G	NCBI36
NG_007965.1:g.8092A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.326A>G MANE Select	ENSP00000368079.4:p.Glu109Gly
ENST00000378802.4:c.326A>G	ENSP00000368079.4:p.Glu109Gly
NM_207352.3:c.326A>G	NP_997235.3:p.Glu109Gly
XM_005262935.2:c.326A>G	XP_005262992.1:p.Glu109Gly
XM_006714184.2:c.16A>G	XP_006714247.1:p.Ser6Gly
XM_005262935.4:c.326A>G	XP_005262992.1:p.Glu109Gly
XM_017008037.1:c.16A>G	XP_016863526.1:p.Ser6Gly
NM_207352.4:c.326A>G MANE Select	NP_997235.3:p.Glu109Gly