Canonical Allele Identifier: CA1519883925

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1042536092

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200717G>C , CM000666.2:g.186200717G>C	GRCh38
NC_000004.11:g.187121871G>C , CM000666.1:g.187121871G>C	GRCh37
NC_000004.10:g.187358865G>C	NCBI36
NG_007965.1:g.14198G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-440G>C MANE Select	ENSP00000368079.4:n.802-440G>C
ENST00000378802.4:c.802-440G>C	ENSP00000368079.4:n.802-440G>C
ENST00000507209.5:n.1643-440G>C
NM_207352.3:c.802-440G>C	NP_997235.3:n.802-440G>C
XM_005262935.2:c.802-440G>C	XP_005262992.1:n.802-440G>C
XM_006714184.2:c.406-440G>C	XP_006714247.1:n.406-440G>C
XM_005262935.4:c.802-440G>C	XP_005262992.1:n.802-440G>C
XM_017008037.1:c.406-440G>C	XP_016863526.1:n.406-440G>C
NM_207352.4:c.802-440G>C MANE Select	NP_997235.3:n.802-440G>C