Canonical Allele Identifier: CA1071991776

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736450235
• gnomAD v3: 4-186204901-C-CA
• gnomAD v4: 4-186204901-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204904dup , CM000666.2:g.186204904dup	GRCh38
NC_000004.11:g.187126058dup , CM000666.1:g.187126058dup	GRCh37
NC_000004.10:g.187363052dup	NCBI36
NG_007965.1:g.18385dup
NG_012095.2:g.926dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-296dup MANE Select	ENSP00000368079.4:n.988-296dup
ENST00000378802.4:c.988-296dup	ENSP00000368079.4:n.988-296dup
ENST00000502665.1:n.68dup
ENST00000507209.5:n.5390dup
ENST00000513354.5:n.78-296dup
NM_207352.3:c.988-296dup	NP_997235.3:n.988-296dup
XM_005262935.2:c.988-296dup	XP_005262992.1:n.988-296dup
XM_006714184.2:c.592-296dup	XP_006714247.1:n.592-296dup
XM_005262935.4:c.988-296dup	XP_005262992.1:n.988-296dup
XM_017008037.1:c.592-296dup	XP_016863526.1:n.592-296dup
NM_207352.4:c.988-296dup MANE Select	NP_997235.3:n.988-296dup