Canonical Allele Identifier: CA358949198

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1296185641
• gnomAD v2: 4-187126355-G-A
• gnomAD v4: 4-186205201-G-A
• MyVariant Identifiers: chr4:g.187126355G>A (hg19) ; chr4:g.186205201G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205201G>A , CM000666.2:g.186205201G>A	GRCh38
NC_000004.11:g.187126355G>A , CM000666.1:g.187126355G>A	GRCh37
NC_000004.10:g.187363349G>A	NCBI36
NG_007965.1:g.18682G>A
NG_012095.2:g.1223G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.989G>A MANE Select	ENSP00000368079.4:p.Gly330Glu
ENST00000378802.4:c.989G>A	ENSP00000368079.4:p.Gly330Glu
ENST00000502665.1:n.224G>A
ENST00000507209.5:n.5687G>A
ENST00000513354.5:n.79G>A
NM_207352.3:c.989G>A	NP_997235.3:p.Gly330Glu
XM_005262935.2:c.989G>A	XP_005262992.1:p.Gly330Glu
XM_006714184.2:c.593G>A	XP_006714247.1:p.Gly198Glu
XM_005262935.4:c.989G>A	XP_005262992.1:p.Gly330Glu
XM_017008037.1:c.593G>A	XP_016863526.1:p.Gly198Glu
NM_207352.4:c.989G>A MANE Select	NP_997235.3:p.Gly330Glu