Canonical Allele Identifier: CA358946306

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187112978A>T (hg19) ; chr4:g.186191824A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186191824A>T , CM000666.2:g.186191824A>T	GRCh38
NC_000004.11:g.187112978A>T , CM000666.1:g.187112978A>T	GRCh37
NC_000004.10:g.187349972A>T	NCBI36
NG_007965.1:g.5305A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1A>T MANE Select	ENSP00000368079.4:p.Met1Leu
ENST00000378802.4:c.1A>T	ENSP00000368079.4:p.Met1Leu
NM_207352.3:c.1A>T	NP_997235.3:p.Met1Leu
XM_005262935.2:c.1A>T	XP_005262992.1:p.Met1Leu
XM_005262935.4:c.1A>T	XP_005262992.1:p.Met1Leu
XM_017008037.1:c.-310A>T	XP_016863526.1:n.-310A>T
NM_207352.4:c.1A>T MANE Select	NP_997235.3:p.Met1Leu