Canonical Allele Identifier: CA358949893

Gene: CYP4V2

Linked Data

• ClinVar Variation Id: 2131760
• ClinVar RCV Id: RCV003036414
• MyVariant Identifiers: chr4:g.187130028A>G (hg19) ; chr4:g.186208874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208874A>G , CM000666.2:g.186208874A>G	GRCh38
NC_000004.11:g.187130028A>G , CM000666.1:g.187130028A>G	GRCh37
NC_000004.10:g.187367022A>G	NCBI36
NG_007965.1:g.22355A>G
NG_012095.2:g.4896A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1100A>G MANE Select	ENSP00000368079.4:p.Asp367Gly
ENST00000378802.4:c.1100A>G	ENSP00000368079.4:p.Asp367Gly
ENST00000502665.1:n.335A>G
ENST00000507209.5:n.5798A>G
ENST00000513354.5:n.190A>G
NM_207352.3:c.1100A>G	NP_997235.3:p.Asp367Gly
XM_005262935.2:c.1100A>G	XP_005262992.1:p.Asp367Gly
XM_006714184.2:c.704A>G	XP_006714247.1:p.Asp235Gly
XM_005262935.4:c.1100A>G	XP_005262992.1:p.Asp367Gly
XM_017008037.1:c.704A>G	XP_016863526.1:p.Asp235Gly
NM_207352.4:c.1100A>G MANE Select	NP_997235.3:p.Asp367Gly