Canonical Allele Identifier: CA2672895955

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204616-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204616C>A , CM000666.2:g.186204616C>A	GRCh38
NC_000004.11:g.187125770C>A , CM000666.1:g.187125770C>A	GRCh37
NC_000004.10:g.187362764C>A	NCBI36
NG_007965.1:g.18097C>A
NG_012095.2:g.638C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-584C>A MANE Select	ENSP00000368079.4:n.988-584C>A
ENST00000378802.4:c.988-584C>A	ENSP00000368079.4:n.988-584C>A
ENST00000507209.5:n.5102C>A
ENST00000513354.5:n.77+159C>A
NM_207352.3:c.988-584C>A	NP_997235.3:n.988-584C>A
XM_005262935.2:c.988-584C>A	XP_005262992.1:n.988-584C>A
XM_006714184.2:c.592-584C>A	XP_006714247.1:n.592-584C>A
XM_005262935.4:c.988-584C>A	XP_005262992.1:n.988-584C>A
XM_017008037.1:c.592-584C>A	XP_016863526.1:n.592-584C>A
NM_207352.4:c.988-584C>A MANE Select	NP_997235.3:n.988-584C>A