Canonical Allele Identifier: CA442638548
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187113082G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191928G>A , CM000666.2:g.186191928G>A GRCh38
NC_000004.11:g.187113082G>A , CM000666.1:g.187113082G>A GRCh37
NC_000004.10:g.187350076G>A NCBI36
NG_007965.1:g.5409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.105G>A MANE Select ENSP00000368079.4:p.Gln35=
ENST00000378802.4:c.105G>A ENSP00000368079.4:p.Gln35=
NM_207352.3:c.105G>A NP_997235.3:p.Gln35=
XM_005262935.2:c.105G>A XP_005262992.1:p.Gln35=
XM_005262935.4:c.105G>A XP_005262992.1:p.Gln35=
XM_017008037.1:c.-206G>A XP_016863526.1:n.-206G>A
NM_207352.4:c.105G>A MANE Select NP_997235.3:p.Gln35=
Search 100 bp 5'
Search 100 bp 3'