Canonical Allele Identifier: CA1215986838
Gene: RGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812010T= , CM000663.2:g.192812010T= GRCh38
NC_000001.10:g.192781140T= , CM000663.1:g.192781140T= GRCh37
NC_000001.9:g.191047763T= NCBI36
NG_012800.1:g.7972T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*414T= MANE Select ENSP00000235382.5:n.*414T=
ENST00000235382.6:c.*414T= ENSP00000235382.5:n.*414T=
NM_002923.3:c.*414T= NP_002914.1:n.*414T=
NM_002923.4:c.*414T= MANE Select NP_002914.1:n.*414T=
Search 100 bp 5'
Search 100 bp 3'