Canonical Allele Identifier: CA557054531

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1452370661
• gnomAD v2: 4-187126314-A-G
• gnomAD v4: 4-186205160-A-G
• MyVariant Identifiers: chr4:g.187126314A>G (hg19) ; chr4:g.186205160A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205160A>G , CM000666.2:g.186205160A>G	GRCh38
NC_000004.11:g.187126314A>G , CM000666.1:g.187126314A>G	GRCh37
NC_000004.10:g.187363308A>G	NCBI36
NG_007965.1:g.18641A>G
NG_012095.2:g.1182A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-40A>G MANE Select	ENSP00000368079.4:n.988-40A>G
ENST00000378802.4:c.988-40A>G	ENSP00000368079.4:n.988-40A>G
ENST00000502665.1:n.223-40A>G
ENST00000507209.5:n.5646A>G
ENST00000513354.5:n.78-40A>G
NM_207352.3:c.988-40A>G	NP_997235.3:n.988-40A>G
XM_005262935.2:c.988-40A>G	XP_005262992.1:n.988-40A>G
XM_006714184.2:c.592-40A>G	XP_006714247.1:n.592-40A>G
XM_005262935.4:c.988-40A>G	XP_005262992.1:n.988-40A>G
XM_017008037.1:c.592-40A>G	XP_016863526.1:n.592-40A>G
NM_207352.4:c.988-40A>G MANE Select	NP_997235.3:n.988-40A>G