Canonical Allele Identifier: CA2649611579

Gene: RGS2

Linked Data

• gnomAD v4: 1-192811967-CCTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192811968_192811970del , CM000663.2:g.192811968_192811970del	GRCh38
NC_000001.10:g.192781098_192781100del , CM000663.1:g.192781098_192781100del	GRCh37
NC_000001.9:g.191047721_191047723del	NCBI36
NG_012800.1:g.7930_7932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*372_*374del MANE Select	ENSP00000235382.5:n.*372_*374del
ENST00000235382.6:c.*372_*374del	ENSP00000235382.5:n.*372_*374del
NM_002923.3:c.*372_*374del	NP_002914.1:n.*372_*374del
NM_002923.4:c.*372_*374del MANE Select	NP_002914.1:n.*372_*374del