Canonical Allele Identifier: CA1148399731
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812224G= , CM000663.2:g.192812224G= GRCh38
NC_000001.10:g.192781354G= , CM000663.1:g.192781354G= GRCh37
NC_000001.9:g.191047977G= NCBI36
NG_012800.1:g.8186G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*628G= MANE Select ENSP00000235382.5:n.*628G=
ENST00000235382.6:c.*628G= ENSP00000235382.5:n.*628G=
NM_002923.3:c.*628G= NP_002914.1:n.*628G=
NM_002923.4:c.*628G= MANE Select NP_002914.1:n.*628G=