Canonical Allele Identifier: CA2270725137

Gene: RGS9

Linked Data

• dbSNP Id: rs1598611632

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65201822T>G , CM000679.2:g.65201822T>G	GRCh38
NC_000017.10:g.63197940T>G , CM000679.1:g.63197940T>G	GRCh37
NC_000017.9:g.60628402T>G	NCBI36
NG_013021.1:g.69485T>G
NG_013021.2:g.69485T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262406.10:c.977-171T>G MANE Select	ENSP00000262406.9:n.977-171T>G
ENST00000635833.1:c.977-171T>G	ENSP00000490658.1:n.977-171T>G
ENST00000262406.9:c.977-171T>G	ENSP00000262406.9:n.977-171T>G
ENST00000443584.7:c.968-171T>G	ENSP00000405814.3:n.968-171T>G
ENST00000449996.7:c.968-171T>G	ENSP00000396329.3:n.968-171T>G
ENST00000577595.1:n.905-171T>G
ENST00000581175.5:n.985-171T>G
ENST00000584234.5:c.977-171T>G	ENSP00000463410.1:n.977-171T>G
NM_001081955.2:c.968-171T>G	NP_001075424.1:n.968-171T>G
NM_001165933.1:c.968-171T>G	NP_001159405.1:n.968-171T>G
NM_003835.3:c.977-171T>G	NP_003826.2:n.977-171T>G
XM_011525426.1:c.389-171T>G	XP_011523728.1:n.389-171T>G
XM_011525426.3:c.389-171T>G	XP_011523728.1:n.389-171T>G
NM_003835.4:c.977-171T>G MANE Select	NP_003826.2:n.977-171T>G
NM_001081955.3:c.968-171T>G	NP_001075424.1:n.968-171T>G
NM_001165933.2:c.968-171T>G	NP_001159405.1:n.968-171T>G