Canonical Allele Identifier: CA35070414
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs3835598

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812265_192812268del , CM000663.2:g.192812265_192812268del GRCh38
NC_000001.10:g.192781395_192781398del , CM000663.1:g.192781395_192781398del GRCh37
NC_000001.9:g.191048018_191048021del NCBI36
NG_012800.1:g.8227_8230del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*669_*672del MANE Select ENSP00000235382.5:n.*669_*672del
ENST00000235382.6:c.*669_*672del ENSP00000235382.5:n.*669_*672del
NM_002923.3:c.*669_*672del NP_002914.1:n.*669_*672del
NM_002923.4:c.*669_*672del MANE Select NP_002914.1:n.*669_*672del