Canonical Allele Identifier: CA2649611475
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811821_192811829del , CM000663.2:g.192811821_192811829del GRCh38
NC_000001.10:g.192780951_192780959del , CM000663.1:g.192780951_192780959del GRCh37
NC_000001.9:g.191047574_191047582del NCBI36
NG_012800.1:g.7783_7791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*225_*233del MANE Select ENSP00000235382.5:n.*225_*233del
ENST00000235382.6:c.*225_*233del ENSP00000235382.5:n.*225_*233del
NM_002923.3:c.*225_*233del NP_002914.1:n.*225_*233del
NM_002923.4:c.*225_*233del MANE Select NP_002914.1:n.*225_*233del