Canonical Allele Identifier: CA3162653

Gene: CYP4V2

Linked Data

• dbSNP Id: rs751298422
• ExAC: 4:187120279 C / G
• gnomAD v2: 4-187120279-C-G
• gnomAD v4: 4-186199125-C-G
• MyVariant Identifiers: chr4:g.187120279C>G (hg19) ; chr4:g.186199125C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199125C>G , CM000666.2:g.186199125C>G	GRCh38
NC_000004.11:g.187120279C>G , CM000666.1:g.187120279C>G	GRCh37
NC_000004.10:g.187357273C>G	NCBI36
NG_007965.1:g.12606C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.801+42C>G MANE Select	ENSP00000368079.4:n.801+42C>G
ENST00000378802.4:c.801+42C>G	ENSP00000368079.4:n.801+42C>G
ENST00000507209.5:n.1642+42C>G
NM_207352.3:c.801+42C>G	NP_997235.3:n.801+42C>G
XM_005262935.2:c.801+42C>G	XP_005262992.1:n.801+42C>G
XM_006714184.2:c.405+42C>G	XP_006714247.1:n.405+42C>G
XM_005262935.4:c.801+42C>G	XP_005262992.1:n.801+42C>G
XM_017008037.1:c.405+42C>G	XP_016863526.1:n.405+42C>G
NM_207352.4:c.801+42C>G MANE Select	NP_997235.3:n.801+42C>G