Canonical Allele Identifier: CA729320729
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1239938244
MyVariant Identifiers: chr1:g.192781394A>C (hg19) chr1:g.192812264A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812264A>C , CM000663.2:g.192812264A>C GRCh38
NC_000001.10:g.192781394A>C , CM000663.1:g.192781394A>C GRCh37
NC_000001.9:g.191048017A>C NCBI36
NG_012800.1:g.8226A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*668A>C MANE Select ENSP00000235382.5:n.*668A>C
ENST00000235382.6:c.*668A>C ENSP00000235382.5:n.*668A>C
NM_002923.3:c.*668A>C NP_002914.1:n.*668A>C
NM_002923.4:c.*668A>C MANE Select NP_002914.1:n.*668A>C
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