Canonical Allele Identifier: CA1519884214

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1579967506
• gnomAD v4: 4-186201097-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186201097G>T , CM000666.2:g.186201097G>T	GRCh38
NC_000004.11:g.187122251G>T , CM000666.1:g.187122251G>T	GRCh37
NC_000004.10:g.187359245G>T	NCBI36
NG_007965.1:g.14578G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.802-60G>T MANE Select	ENSP00000368079.4:n.802-60G>T
ENST00000378802.4:c.802-60G>T	ENSP00000368079.4:n.802-60G>T
ENST00000507209.5:n.1643-60G>T
NM_207352.3:c.802-60G>T	NP_997235.3:n.802-60G>T
XM_005262935.2:c.802-60G>T	XP_005262992.1:n.802-60G>T
XM_006714184.2:c.406-60G>T	XP_006714247.1:n.406-60G>T
XM_005262935.4:c.802-60G>T	XP_005262992.1:n.802-60G>T
XM_017008037.1:c.406-60G>T	XP_016863526.1:n.406-60G>T
NM_207352.4:c.802-60G>T MANE Select	NP_997235.3:n.802-60G>T