Canonical Allele Identifier: CA112131762

Gene: CYP4V2

Linked Data

• dbSNP Id: rs759552576
• gnomAD v4: 4-186205327-A-G
• MyVariant Identifiers: chr4:g.187126481A>G (hg19) ; chr4:g.186205327A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205327A>G , CM000666.2:g.186205327A>G	GRCh38
NC_000004.11:g.187126481A>G , CM000666.1:g.187126481A>G	GRCh37
NC_000004.10:g.187363475A>G	NCBI36
NG_007965.1:g.18808A>G
NG_012095.2:g.1349A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+25A>G MANE Select	ENSP00000368079.4:n.1090+25A>G
ENST00000378802.4:c.1090+25A>G	ENSP00000368079.4:n.1090+25A>G
ENST00000502665.1:n.325+25A>G
ENST00000507209.5:n.5788+25A>G
ENST00000513354.5:n.180+25A>G
NM_207352.3:c.1090+25A>G	NP_997235.3:n.1090+25A>G
XM_005262935.2:c.1090+25A>G	XP_005262992.1:n.1090+25A>G
XM_006714184.2:c.694+25A>G	XP_006714247.1:n.694+25A>G
XM_005262935.4:c.1090+25A>G	XP_005262992.1:n.1090+25A>G
XM_017008037.1:c.694+25A>G	XP_016863526.1:n.694+25A>G
NM_207352.4:c.1090+25A>G MANE Select	NP_997235.3:n.1090+25A>G