Canonical Allele Identifier: CA2270725146

Gene: RGS9

Linked Data

• dbSNP Id: rs1598611657
• gnomAD v4: 17-65201846-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65201846G>T , CM000679.2:g.65201846G>T	GRCh38
NC_000017.10:g.63197964G>T , CM000679.1:g.63197964G>T	GRCh37
NC_000017.9:g.60628426G>T	NCBI36
NG_013021.1:g.69509G>T
NG_013021.2:g.69509G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262406.10:c.977-147G>T MANE Select	ENSP00000262406.9:n.977-147G>T
ENST00000635833.1:c.977-147G>T	ENSP00000490658.1:n.977-147G>T
ENST00000262406.9:c.977-147G>T	ENSP00000262406.9:n.977-147G>T
ENST00000443584.7:c.968-147G>T	ENSP00000405814.3:n.968-147G>T
ENST00000449996.7:c.968-147G>T	ENSP00000396329.3:n.968-147G>T
ENST00000577595.1:n.905-147G>T
ENST00000581175.5:n.985-147G>T
ENST00000584234.5:c.977-147G>T	ENSP00000463410.1:n.977-147G>T
NM_001081955.2:c.968-147G>T	NP_001075424.1:n.968-147G>T
NM_001165933.1:c.968-147G>T	NP_001159405.1:n.968-147G>T
NM_003835.3:c.977-147G>T	NP_003826.2:n.977-147G>T
XM_011525426.1:c.389-147G>T	XP_011523728.1:n.389-147G>T
XM_011525426.3:c.389-147G>T	XP_011523728.1:n.389-147G>T
NM_003835.4:c.977-147G>T MANE Select	NP_003826.2:n.977-147G>T
NM_001081955.3:c.968-147G>T	NP_001075424.1:n.968-147G>T
NM_001165933.2:c.968-147G>T	NP_001159405.1:n.968-147G>T