Canonical Allele Identifier: CA2649611501
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811854_192811855insTACCAAATAAACAACTTTTTTGTTTTATTTCAG , CM000663.2:g.192811854_192811855insTACCAAATAAACAACTTTTTTGTTTTATTTCAG GRCh38
NC_000001.10:g.192780984_192780985insTACCAAATAAACAACTTTTTTGTTTTATTTCAG , CM000663.1:g.192780984_192780985insTACCAAATAAACAACTTTTTTGTTTTATTTCAG GRCh37
NC_000001.9:g.191047607_191047608insTACCAAATAAACAACTTTTTTGTTTTATTTCAG NCBI36
NG_012800.1:g.7816_7817insTACCAAATAAACAACTTTTTTGTTTTATTTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATTTCAG MANE Select ENSP00000235382.5:n.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATT...
ENST00000235382.6:c.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATTTCAG ENSP00000235382.5:n.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATT...
NM_002923.3:c.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATTTCAG NP_002914.1:n.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATTTCAG
NM_002923.4:c.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATTTCAG MANE Select NP_002914.1:n.*258_*259insTACCAAATAAACAACTTTTTTGTTTTATTTCAG