Canonical Allele Identifier: CA112120761

Gene: CYP4V2

Linked Data

• dbSNP Id: rs184324338
• MyVariant Identifiers: chr4:g.186194220G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194220G>T , CM000666.2:g.186194220G>T	GRCh38
NC_000004.11:g.187115374G>T , CM000666.1:g.187115374G>T	GRCh37
NC_000004.10:g.187352368G>T	NCBI36
NG_007965.1:g.7701G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.215-280G>T MANE Select	ENSP00000368079.4:n.215-280G>T
ENST00000378802.4:c.215-280G>T	ENSP00000368079.4:n.215-280G>T
NM_207352.3:c.215-280G>T	NP_997235.3:n.215-280G>T
XM_005262935.2:c.215-280G>T	XP_005262992.1:n.215-280G>T
XM_005262935.4:c.215-280G>T	XP_005262992.1:n.215-280G>T
XM_017008037.1:c.-96-280G>T	XP_016863526.1:n.-96-280G>T
NM_207352.4:c.215-280G>T MANE Select	NP_997235.3:n.215-280G>T