Canonical Allele Identifier: CA358946788

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186194499-G-A
• MyVariant Identifiers: chr4:g.187115653G>A (hg19) ; chr4:g.186194499G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194499G>A , CM000666.2:g.186194499G>A	GRCh38
NC_000004.11:g.187115653G>A , CM000666.1:g.187115653G>A	GRCh37
NC_000004.10:g.187352647G>A	NCBI36
NG_007965.1:g.7980G>A

Transcript Alleles

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