Canonical Allele Identifier: CA646208662
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811662dup , CM000663.2:g.192811662dup GRCh38
NC_000001.10:g.192780792dup , CM000663.1:g.192780792dup GRCh37
NC_000001.9:g.191047415dup NCBI36
NG_012800.1:g.7624dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*66dup MANE Select ENSP00000235382.5:n.*66dup
ENST00000235382.6:c.*66dup ENSP00000235382.5:n.*66dup
NM_002923.3:c.*66dup NP_002914.1:n.*66dup
NM_002923.4:c.*66dup MANE Select NP_002914.1:n.*66dup