Canonical Allele Identifier: CA3162651

Gene: CYP4V2

Linked Data

• dbSNP Id: rs758339688
• ExAC: 4:187120274 C / A
• gnomAD v2: 4-187120274-C-A
• gnomAD v4: 4-186199120-C-A
• MyVariant Identifiers: chr4:g.187120274C>A (hg19) ; chr4:g.186199120C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199120C>A , CM000666.2:g.186199120C>A	GRCh38
NC_000004.11:g.187120274C>A , CM000666.1:g.187120274C>A	GRCh37
NC_000004.10:g.187357268C>A	NCBI36
NG_007965.1:g.12601C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.801+37C>A MANE Select	ENSP00000368079.4:n.801+37C>A
ENST00000378802.4:c.801+37C>A	ENSP00000368079.4:n.801+37C>A
ENST00000507209.5:n.1642+37C>A
NM_207352.3:c.801+37C>A	NP_997235.3:n.801+37C>A
XM_005262935.2:c.801+37C>A	XP_005262992.1:n.801+37C>A
XM_006714184.2:c.405+37C>A	XP_006714247.1:n.405+37C>A
XM_005262935.4:c.801+37C>A	XP_005262992.1:n.801+37C>A
XM_017008037.1:c.405+37C>A	XP_016863526.1:n.405+37C>A
NM_207352.4:c.801+37C>A MANE Select	NP_997235.3:n.801+37C>A