Canonical Allele Identifier: CA528004656
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1397062471
gnomAD v2: 1-192781318-A-G
gnomAD v3: 1-192812188-A-G
gnomAD v4: 1-192812188-A-G
MyVariant Identifiers: chr1:g.192781318A>G (hg19) chr1:g.192812188A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812188A>G , CM000663.2:g.192812188A>G GRCh38
NC_000001.10:g.192781318A>G , CM000663.1:g.192781318A>G GRCh37
NC_000001.9:g.191047941A>G NCBI36
NG_012800.1:g.8150A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*592A>G MANE Select ENSP00000235382.5:n.*592A>G
ENST00000235382.6:c.*592A>G ENSP00000235382.5:n.*592A>G
NM_002923.3:c.*592A>G NP_002914.1:n.*592A>G
NM_002923.4:c.*592A>G MANE Select NP_002914.1:n.*592A>G
Search 100 bp 5'
Search 100 bp 3'