Canonical Allele Identifier: CA729320515
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs868053520
gnomAD v3: 1-192811836-C-G
gnomAD v4: 1-192811836-C-G
MyVariant Identifiers: chr1:g.192780966C>G (hg19) chr1:g.192811836C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811836C>G , CM000663.2:g.192811836C>G GRCh38
NC_000001.10:g.192780966C>G , CM000663.1:g.192780966C>G GRCh37
NC_000001.9:g.191047589C>G NCBI36
NG_012800.1:g.7798C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*240C>G MANE Select ENSP00000235382.5:n.*240C>G
ENST00000235382.6:c.*240C>G ENSP00000235382.5:n.*240C>G
NM_002923.3:c.*240C>G NP_002914.1:n.*240C>G
NM_002923.4:c.*240C>G MANE Select NP_002914.1:n.*240C>G
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