Canonical Allele Identifier: CA442640858
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187126365A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205211A>T , CM000666.2:g.186205211A>T GRCh38
NC_000004.11:g.187126365A>T , CM000666.1:g.187126365A>T GRCh37
NC_000004.10:g.187363359A>T NCBI36
NG_007965.1:g.18692A>T
NG_012095.2:g.1233A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.999A>T MANE Select ENSP00000368079.4:p.Thr333=
ENST00000378802.4:c.999A>T ENSP00000368079.4:p.Thr333=
ENST00000502665.1:n.234A>T
ENST00000507209.5:n.5697A>T
ENST00000513354.5:n.89A>T
NM_207352.3:c.999A>T NP_997235.3:p.Thr333=
XM_005262935.2:c.999A>T XP_005262992.1:p.Thr333=
XM_006714184.2:c.603A>T XP_006714247.1:p.Thr201=
XM_005262935.4:c.999A>T XP_005262992.1:p.Thr333=
XM_017008037.1:c.603A>T XP_016863526.1:p.Thr201=
NM_207352.4:c.999A>T MANE Select NP_997235.3:p.Thr333=