Canonical Allele Identifier: CA2649611452
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811779-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811779A>C , CM000663.2:g.192811779A>C GRCh38
NC_000001.10:g.192780909A>C , CM000663.1:g.192780909A>C GRCh37
NC_000001.9:g.191047532A>C NCBI36
NG_012800.1:g.7741A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*183A>C MANE Select ENSP00000235382.5:n.*183A>C
ENST00000235382.6:c.*183A>C ENSP00000235382.5:n.*183A>C
NM_002923.3:c.*183A>C NP_002914.1:n.*183A>C
NM_002923.4:c.*183A>C MANE Select NP_002914.1:n.*183A>C
Search 100 bp 5'
Search 100 bp 3'