Canonical Allele Identifier: CA1215986939

Gene: RGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192812250_192812254delinsAATTT , CM000663.2:g.192812250_192812254delinsAATTT	GRCh38
NC_000001.10:g.192781380_192781384delinsAATTT , CM000663.1:g.192781380_192781384delinsAATTT	GRCh37
NC_000001.9:g.191048003_191048007delinsAATTT	NCBI36
NG_012800.1:g.8212_8216delinsAATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*654_*658delinsAATTT MANE Select	ENSP00000235382.5:n.*654_*658delinsAATTT
ENST00000235382.6:c.*654_*658delinsAATTT	ENSP00000235382.5:n.*654_*658delinsAATTT
NM_002923.3:c.*654_*658delinsAATTT	NP_002914.1:n.*654_*658delinsAATTT
NM_002923.4:c.*654_*658delinsAATTT MANE Select	NP_002914.1:n.*654_*658delinsAATTT