Canonical Allele Identifier: CA358946920

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187115711A>T (hg19) ; chr4:g.186194557A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194557A>T , CM000666.2:g.186194557A>T	GRCh38
NC_000004.11:g.187115711A>T , CM000666.1:g.187115711A>T	GRCh37
NC_000004.10:g.187352705A>T	NCBI36
NG_007965.1:g.8038A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.272A>T MANE Select	ENSP00000368079.4:p.Lys91Met
ENST00000378802.4:c.272A>T	ENSP00000368079.4:p.Lys91Met
NM_207352.3:c.272A>T	NP_997235.3:p.Lys91Met
XM_005262935.2:c.272A>T	XP_005262992.1:p.Lys91Met
XM_006714184.2:c.-39A>T	XP_006714247.1:n.-39A>T
XM_005262935.4:c.272A>T	XP_005262992.1:p.Lys91Met
XM_017008037.1:c.-39A>T	XP_016863526.1:n.-39A>T
NM_207352.4:c.272A>T MANE Select	NP_997235.3:p.Lys91Met