Canonical Allele Identifier: CA358950266

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736618612
• MyVariant Identifiers: chr4:g.187130120T>G (hg19) ; chr4:g.186208966T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208966T>G , CM000666.2:g.186208966T>G	GRCh38
NC_000004.11:g.187130120T>G , CM000666.1:g.187130120T>G	GRCh37
NC_000004.10:g.187367114T>G	NCBI36
NG_007965.1:g.22447T>G
NG_012095.2:g.4988T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1192T>G MANE Select	ENSP00000368079.4:p.Phe398Val
ENST00000378802.4:c.1192T>G	ENSP00000368079.4:p.Phe398Val
ENST00000502665.1:n.427T>G
ENST00000507209.5:n.5890T>G
ENST00000513354.5:n.282T>G
NM_207352.3:c.1192T>G	NP_997235.3:p.Phe398Val
XM_005262935.2:c.1192T>G	XP_005262992.1:p.Phe398Val
XM_006714184.2:c.796T>G	XP_006714247.1:p.Phe266Val
XM_005262935.4:c.1192T>G	XP_005262992.1:p.Phe398Val
XM_017008037.1:c.796T>G	XP_016863526.1:p.Phe266Val
NM_207352.4:c.1192T>G MANE Select	NP_997235.3:p.Phe398Val