Canonical Allele Identifier: CA400673407

Gene: RGS9

Linked Data

• ClinVar Variation Id: 1471896
• ClinVar RCV Id: RCV002002764
• dbSNP Id: rs34797451
• MyVariant Identifiers: chr17:g.63221214G>T (hg19) ; chr17:g.65225096G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65225096G>T , CM000679.2:g.65225096G>T	GRCh38
NC_000017.10:g.63221214G>T , CM000679.1:g.63221214G>T	GRCh37
NC_000017.9:g.60651676G>T	NCBI36
NG_013021.1:g.92759G>T
NG_013021.2:g.92759G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262406.10:c.1502G>T MANE Select	ENSP00000262406.9:p.Arg501Leu
ENST00000635833.1:c.1502G>T	ENSP00000490658.1:p.Arg501Leu
ENST00000262406.9:c.1502G>T	ENSP00000262406.9:p.Arg501Leu
ENST00000443584.7:c.1493G>T	ENSP00000405814.3:p.Arg498Leu
ENST00000449996.7:c.1493G>T	ENSP00000396329.3:p.Arg498Leu
ENST00000577595.1:n.1430G>T
ENST00000584234.5:c.*21G>T	ENSP00000463410.1:n.*21G>T
NM_001081955.2:c.1493G>T	NP_001075424.1:p.Arg498Leu
NM_003835.3:c.1502G>T	NP_003826.2:p.Arg501Leu
XM_011525426.1:c.914G>T	XP_011523728.1:p.Arg305Leu
XM_011525426.3:c.914G>T	XP_011523728.1:p.Arg305Leu
NM_003835.4:c.1502G>T MANE Select	NP_003826.2:p.Arg501Leu
NM_001081955.3:c.1493G>T	NP_001075424.1:p.Arg498Leu