Canonical Allele Identifier: CA792318010

Gene: CYP4V2

Linked Data

• dbSNP Id: rs528660295
• gnomAD v3: 4-186194716-C-CA
• gnomAD v4: 4-186194716-C-CA
• MyVariant Identifiers: chr4:g.187115870_187115871insA (hg19) ; chr4:g.186194716_186194717insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194722dup , CM000666.2:g.186194722dup	GRCh38
NC_000004.11:g.187115876dup , CM000666.1:g.187115876dup	GRCh37
NC_000004.10:g.187352870dup	NCBI36
NG_007965.1:g.8203dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+110dup MANE Select	ENSP00000368079.4:n.327+110dup
ENST00000378802.4:c.327+110dup	ENSP00000368079.4:n.327+110dup
NM_207352.3:c.327+110dup	NP_997235.3:n.327+110dup
XM_005262935.2:c.327+110dup	XP_005262992.1:n.327+110dup
XM_006714184.2:c.17+110dup	XP_006714247.1:n.17+110dup
XM_005262935.4:c.327+110dup	XP_005262992.1:n.327+110dup
XM_017008037.1:c.17+110dup	XP_016863526.1:n.17+110dup
NM_207352.4:c.327+110dup MANE Select	NP_997235.3:n.327+110dup