Canonical Allele Identifier: CA2649611382
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811675_192811676del , CM000663.2:g.192811675_192811676del GRCh38
NC_000001.10:g.192780805_192780806del , CM000663.1:g.192780805_192780806del GRCh37
NC_000001.9:g.191047428_191047429del NCBI36
NG_012800.1:g.7637_7638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*79_*80del MANE Select ENSP00000235382.5:n.*79_*80del
ENST00000235382.6:c.*79_*80del ENSP00000235382.5:n.*79_*80del
NM_002923.3:c.*79_*80del NP_002914.1:n.*79_*80del
NM_002923.4:c.*79_*80del MANE Select NP_002914.1:n.*79_*80del