Canonical Allele Identifier: CA35070388
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1000453568
MyVariant Identifiers: chr1:g.192781182_192781189del (hg19) chr1:g.192812052_192812059del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812053_192812060del , CM000663.2:g.192812053_192812060del GRCh38
NC_000001.10:g.192781183_192781190del , CM000663.1:g.192781183_192781190del GRCh37
NC_000001.9:g.191047806_191047813del NCBI36
NG_012800.1:g.8015_8022del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*457_*464del MANE Select ENSP00000235382.5:n.*457_*464del
ENST00000235382.6:c.*457_*464del ENSP00000235382.5:n.*457_*464del
NM_002923.3:c.*457_*464del NP_002914.1:n.*457_*464del
NM_002923.4:c.*457_*464del MANE Select NP_002914.1:n.*457_*464del
Search 100 bp 5'
Search 100 bp 3'