Canonical Allele Identifier: CA2649611424
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811749del , CM000663.2:g.192811749del GRCh38
NC_000001.10:g.192780879del , CM000663.1:g.192780879del GRCh37
NC_000001.9:g.191047502del NCBI36
NG_012800.1:g.7711del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*153del MANE Select ENSP00000235382.5:n.*153del
ENST00000235382.6:c.*153del ENSP00000235382.5:n.*153del
NM_002923.3:c.*153del NP_002914.1:n.*153del
NM_002923.4:c.*153del MANE Select NP_002914.1:n.*153del