Canonical Allele Identifier: CA2649611648
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192812050-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812050A>C , CM000663.2:g.192812050A>C GRCh38
NC_000001.10:g.192781180A>C , CM000663.1:g.192781180A>C GRCh37
NC_000001.9:g.191047803A>C NCBI36
NG_012800.1:g.8012A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000235382.7:c.*454A>C MANE Select ENSP00000235382.5:n.*454A>C
ENST00000235382.6:c.*454A>C ENSP00000235382.5:n.*454A>C
NM_002923.3:c.*454A>C NP_002914.1:n.*454A>C
NM_002923.4:c.*454A>C MANE Select NP_002914.1:n.*454A>C
Search 100 bp 5'
Search 100 bp 3'