Canonical Allele Identifier: CA3162716
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs372357833

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205159C>T , CM000666.2:g.186205159C>T GRCh38
NC_000004.11:g.187126313C>T , CM000666.1:g.187126313C>T GRCh37
NC_000004.10:g.187363307C>T NCBI36
NG_007965.1:g.18640C>T
NG_012095.2:g.1181C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-41C>T MANE Select ENSP00000368079.4:p.=
ENST00000378802.4:c.988-41C>T ENSP00000368079.4:p.=
ENST00000502665.1:n.223-41C>T
ENST00000507209.5:n.5645C>T
ENST00000513354.5:n.78-41C>T
NM_207352.3:c.988-41C>T NP_997235.3:p.=
XM_005262935.2:c.988-41C>T XP_005262992.1:p.=
XM_006714184.2:c.592-41C>T XP_006714247.1:p.=
XM_005262935.4:c.988-41C>T XP_005262992.1:p.=
XM_017008037.1:c.592-41C>T XP_016863526.1:p.=
NM_207352.4:c.988-41C>T MANE Select NP_997235.3:p.=