Canonical Allele Identifier: CA112131318

Gene: CYP4V2

Linked Data

• dbSNP Id: rs929827603
• gnomAD v3: 4-186204874-C-T
• gnomAD v4: 4-186204874-C-T
• MyVariant Identifiers: chr4:g.187126028C>T (hg19) ; chr4:g.186204874C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204874C>T , CM000666.2:g.186204874C>T	GRCh38
NC_000004.11:g.187126028C>T , CM000666.1:g.187126028C>T	GRCh37
NC_000004.10:g.187363022C>T	NCBI36
NG_007965.1:g.18355C>T
NG_012095.2:g.896C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-326C>T MANE Select	ENSP00000368079.4:n.988-326C>T
ENST00000378802.4:c.988-326C>T	ENSP00000368079.4:n.988-326C>T
ENST00000502665.1:n.38C>T
ENST00000507209.5:n.5360C>T
ENST00000513354.5:n.78-326C>T
NM_207352.3:c.988-326C>T	NP_997235.3:n.988-326C>T
XM_005262935.2:c.988-326C>T	XP_005262992.1:n.988-326C>T
XM_006714184.2:c.592-326C>T	XP_006714247.1:n.592-326C>T
XM_005262935.4:c.988-326C>T	XP_005262992.1:n.988-326C>T
XM_017008037.1:c.592-326C>T	XP_016863526.1:n.592-326C>T
NM_207352.4:c.988-326C>T MANE Select	NP_997235.3:n.988-326C>T