Canonical Allele Identifier: CA358949222

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187126363A>T (hg19) ; chr4:g.186205209A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205209A>T , CM000666.2:g.186205209A>T	GRCh38
NC_000004.11:g.187126363A>T , CM000666.1:g.187126363A>T	GRCh37
NC_000004.10:g.187363357A>T	NCBI36
NG_007965.1:g.18690A>T
NG_012095.2:g.1231A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.997A>T MANE Select	ENSP00000368079.4:p.Thr333Ser
ENST00000378802.4:c.997A>T	ENSP00000368079.4:p.Thr333Ser
ENST00000502665.1:n.232A>T
ENST00000507209.5:n.5695A>T
ENST00000513354.5:n.87A>T
NM_207352.3:c.997A>T	NP_997235.3:p.Thr333Ser
XM_005262935.2:c.997A>T	XP_005262992.1:p.Thr333Ser
XM_006714184.2:c.601A>T	XP_006714247.1:p.Thr201Ser
XM_005262935.4:c.997A>T	XP_005262992.1:p.Thr333Ser
XM_017008037.1:c.601A>T	XP_016863526.1:p.Thr201Ser
NM_207352.4:c.997A>T MANE Select	NP_997235.3:p.Thr333Ser