Canonical Allele Identifier: CA2672897308

Gene: CYP4V2

Linked Data

• dbSNP Id: rs2126585355
• gnomAD v4: 4-186197277-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197278dup , CM000666.2:g.186197278dup	GRCh38
NC_000004.11:g.187118432dup , CM000666.1:g.187118432dup	GRCh37
NC_000004.10:g.187355426dup	NCBI36
NG_007965.1:g.10759dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+148dup MANE Select	ENSP00000368079.4:n.604+148dup
ENST00000378802.4:c.604+148dup	ENSP00000368079.4:n.604+148dup
ENST00000507209.5:n.1191dup
NM_207352.3:c.604+148dup	NP_997235.3:n.604+148dup
XM_005262935.2:c.604+148dup	XP_005262992.1:n.604+148dup
XM_006714184.2:c.208+148dup	XP_006714247.1:n.208+148dup
XM_005262935.4:c.604+148dup	XP_005262992.1:n.604+148dup
XM_017008037.1:c.208+148dup	XP_016863526.1:n.208+148dup
NM_207352.4:c.604+148dup MANE Select	NP_997235.3:n.604+148dup