Canonical Allele Identifier: CA1010583229
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665594773
gnomAD v3: 1-192811645-A-AG
gnomAD v4: 1-192811645-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811649dup , CM000663.2:g.192811649dup GRCh38
NC_000001.10:g.192780779dup , CM000663.1:g.192780779dup GRCh37
NC_000001.9:g.191047402dup NCBI36
NG_012800.1:g.7611dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*53dup MANE Select ENSP00000235382.5:n.*53dup
ENST00000235382.6:c.*53dup ENSP00000235382.5:n.*53dup
NM_002923.3:c.*53dup NP_002914.1:n.*53dup
NM_002923.4:c.*53dup MANE Select NP_002914.1:n.*53dup
Search 100 bp 5'
Search 100 bp 3'