Canonical Allele Identifier: CA358947556

Gene: CYP4V2

Linked Data

• dbSNP Id: rs758719879
• gnomAD v3: 4-186197080-C-G
• gnomAD v4: 4-186197080-C-G
• MyVariant Identifiers: chr4:g.187118234C>G (hg19) ; chr4:g.186197080C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197080C>G , CM000666.2:g.186197080C>G	GRCh38
NC_000004.11:g.187118234C>G , CM000666.1:g.187118234C>G	GRCh37
NC_000004.10:g.187355228C>G	NCBI36
NG_007965.1:g.10561C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.554C>G MANE Select	ENSP00000368079.4:p.Ala185Gly
ENST00000378802.4:c.554C>G	ENSP00000368079.4:p.Ala185Gly
ENST00000507209.5:n.993C>G
NM_207352.3:c.554C>G	NP_997235.3:p.Ala185Gly
XM_005262935.2:c.554C>G	XP_005262992.1:p.Ala185Gly
XM_006714184.2:c.158C>G	XP_006714247.1:p.Ala53Gly
XM_005262935.4:c.554C>G	XP_005262992.1:p.Ala185Gly
XM_017008037.1:c.158C>G	XP_016863526.1:p.Ala53Gly
NM_207352.4:c.554C>G MANE Select	NP_997235.3:p.Ala185Gly