Canonical Allele Identifier: CA2672892276

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186191816-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186191816C>G , CM000666.2:g.186191816C>G	GRCh38
NC_000004.11:g.187112970C>G , CM000666.1:g.187112970C>G	GRCh37
NC_000004.10:g.187349964C>G	NCBI36
NG_007965.1:g.5297C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.-8C>G MANE Select	ENSP00000368079.4:n.-8C>G
ENST00000378802.4:c.-8C>G	ENSP00000368079.4:n.-8C>G
NM_207352.3:c.-8C>G	NP_997235.3:n.-8C>G
XM_005262935.2:c.-8C>G	XP_005262992.1:n.-8C>G
XM_005262935.4:c.-8C>G	XP_005262992.1:n.-8C>G
XM_017008037.1:c.-318C>G	XP_016863526.1:n.-318C>G
NM_207352.4:c.-8C>G MANE Select	NP_997235.3:n.-8C>G