Canonical Allele Identifier: CA2672896827

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186205096-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205096A>C , CM000666.2:g.186205096A>C	GRCh38
NC_000004.11:g.187126250A>C , CM000666.1:g.187126250A>C	GRCh37
NC_000004.10:g.187363244A>C	NCBI36
NG_007965.1:g.18577A>C
NG_012095.2:g.1118A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-104A>C MANE Select	ENSP00000368079.4:n.988-104A>C
ENST00000378802.4:c.988-104A>C	ENSP00000368079.4:n.988-104A>C
ENST00000502665.1:n.222+38A>C
ENST00000507209.5:n.5582A>C
ENST00000513354.5:n.78-104A>C
NM_207352.3:c.988-104A>C	NP_997235.3:n.988-104A>C
XM_005262935.2:c.988-104A>C	XP_005262992.1:n.988-104A>C
XM_006714184.2:c.592-104A>C	XP_006714247.1:n.592-104A>C
XM_005262935.4:c.988-104A>C	XP_005262992.1:n.988-104A>C
XM_017008037.1:c.592-104A>C	XP_016863526.1:n.592-104A>C
NM_207352.4:c.988-104A>C MANE Select	NP_997235.3:n.988-104A>C