Canonical Allele Identifier: CA729320700
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1162311285
MyVariant Identifiers: chr1:g.192781369T>C (hg19) chr1:g.192812239T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812239T>C , CM000663.2:g.192812239T>C GRCh38
NC_000001.10:g.192781369T>C , CM000663.1:g.192781369T>C GRCh37
NC_000001.9:g.191047992T>C NCBI36
NG_012800.1:g.8201T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*643T>C MANE Select ENSP00000235382.5:n.*643T>C
ENST00000235382.6:c.*643T>C ENSP00000235382.5:n.*643T>C
NM_002923.3:c.*643T>C NP_002914.1:n.*643T>C
NM_002923.4:c.*643T>C MANE Select NP_002914.1:n.*643T>C
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