Canonical Allele Identifier: CA358949501

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187126444G>T (hg19) ; chr4:g.186205290G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205290G>T , CM000666.2:g.186205290G>T	GRCh38
NC_000004.11:g.187126444G>T , CM000666.1:g.187126444G>T	GRCh37
NC_000004.10:g.187363438G>T	NCBI36
NG_007965.1:g.18771G>T
NG_012095.2:g.1312G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1078G>T MANE Select	ENSP00000368079.4:p.Asp360Tyr
ENST00000378802.4:c.1078G>T	ENSP00000368079.4:p.Asp360Tyr
ENST00000502665.1:n.313G>T
ENST00000507209.5:n.5776G>T
ENST00000513354.5:n.168G>T
NM_207352.3:c.1078G>T	NP_997235.3:p.Asp360Tyr
XM_005262935.2:c.1078G>T	XP_005262992.1:p.Asp360Tyr
XM_006714184.2:c.682G>T	XP_006714247.1:p.Asp228Tyr
XM_005262935.4:c.1078G>T	XP_005262992.1:p.Asp360Tyr
XM_017008037.1:c.682G>T	XP_016863526.1:p.Asp228Tyr
NM_207352.4:c.1078G>T MANE Select	NP_997235.3:p.Asp360Tyr