Canonical Allele Identifier: CA1010583241
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665595260

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811678_192811688del , CM000663.2:g.192811678_192811688del GRCh38
NC_000001.10:g.192780808_192780818del , CM000663.1:g.192780808_192780818del GRCh37
NC_000001.9:g.191047431_191047441del NCBI36
NG_012800.1:g.7640_7650del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*82_*92del MANE Select ENSP00000235382.5:n.*82_*92del
ENST00000235382.6:c.*82_*92del ENSP00000235382.5:n.*82_*92del
NM_002923.3:c.*82_*92del NP_002914.1:n.*82_*92del
NM_002923.4:c.*82_*92del MANE Select NP_002914.1:n.*82_*92del