Canonical Allele Identifier: CA442639023

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187118259T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197105T>C , CM000666.2:g.186197105T>C	GRCh38
NC_000004.11:g.187118259T>C , CM000666.1:g.187118259T>C	GRCh37
NC_000004.10:g.187355253T>C	NCBI36
NG_007965.1:g.10586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.579T>C MANE Select	ENSP00000368079.4:p.Thr193=
ENST00000378802.4:c.579T>C	ENSP00000368079.4:p.Thr193=
ENST00000507209.5:n.1018T>C
NM_207352.3:c.579T>C	NP_997235.3:p.Thr193=
XM_005262935.2:c.579T>C	XP_005262992.1:p.Thr193=
XM_006714184.2:c.183T>C	XP_006714247.1:p.Thr61=
XM_005262935.4:c.579T>C	XP_005262992.1:p.Thr193=
XM_017008037.1:c.183T>C	XP_016863526.1:p.Thr61=
NM_207352.4:c.579T>C MANE Select	NP_997235.3:p.Thr193=