Canonical Allele Identifier: CA9837401
Gene: ROMO1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35699657G>A , CM000682.2:g.35699657G>A GRCh38
NC_000020.10:g.34287579G>A , CM000682.1:g.34287579G>A GRCh37
NC_000020.9:g.33750993G>A NCBI36
NG_033237.1:g.4709C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374077.8:c.25G>A MANE Select ENSP00000363190.3:p.Gly9Arg
ENST00000336695.4:c.25G>A ENSP00000338293.4:p.Gly9Arg
ENST00000374072.5:c.25G>A ENSP00000363185.1:p.Gly9Arg
ENST00000374077.7:c.25G>A ENSP00000363190.3:p.Gly9Arg
ENST00000374078.5:c.25G>A ENSP00000363191.1:p.Gly9Arg
ENST00000397416.1:c.25G>A ENSP00000380561.1:p.Gly9Arg
NM_080748.2:c.25G>A NP_542786.1:p.Gly9Arg
XM_017027678.1:c.25G>A XP_016883167.1:p.Gly9Arg
NM_080748.3:c.25G>A MANE Select NP_542786.1:p.Gly9Arg