Canonical Allele Identifier: CA358947722

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187118701A>T (hg19) ; chr4:g.186197547A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197547A>T , CM000666.2:g.186197547A>T	GRCh38
NC_000004.11:g.187118701A>T , CM000666.1:g.187118701A>T	GRCh37
NC_000004.10:g.187355695A>T	NCBI36
NG_007965.1:g.11028A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.619A>T MANE Select	ENSP00000368079.4:p.Lys207Ter
ENST00000378802.4:c.619A>T	ENSP00000368079.4:p.Lys207Ter
ENST00000507209.5:n.1460A>T
NM_207352.3:c.619A>T	NP_997235.3:p.Lys207Ter
XM_005262935.2:c.619A>T	XP_005262992.1:p.Lys207Ter
XM_006714184.2:c.223A>T	XP_006714247.1:p.Lys75Ter
XM_005262935.4:c.619A>T	XP_005262992.1:p.Lys207Ter
XM_017008037.1:c.223A>T	XP_016863526.1:p.Lys75Ter
NM_207352.4:c.619A>T MANE Select	NP_997235.3:p.Lys207Ter