Canonical Allele Identifier: CA2747137550
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812198_192812201del , CM000663.2:g.192812198_192812201del GRCh38
NC_000001.10:g.192781328_192781331del , CM000663.1:g.192781328_192781331del GRCh37
NC_000001.9:g.191047951_191047954del NCBI36
NG_012800.1:g.8160_8163del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*602_*605del MANE Select ENSP00000235382.5:n.*602_*605del
ENST00000235382.6:c.*602_*605del ENSP00000235382.5:n.*602_*605del
NM_002923.3:c.*602_*605del NP_002914.1:n.*602_*605del
NM_002923.4:c.*602_*605del MANE Select NP_002914.1:n.*602_*605del