Canonical Allele Identifier: CA2541983857
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811667-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811667A>G , CM000663.2:g.192811667A>G GRCh38
NC_000001.10:g.192780797A>G , CM000663.1:g.192780797A>G GRCh37
NC_000001.9:g.191047420A>G NCBI36
NG_012800.1:g.7629A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*71A>G MANE Select ENSP00000235382.5:n.*71A>G
ENST00000235382.6:c.*71A>G ENSP00000235382.5:n.*71A>G
NM_002923.3:c.*71A>G NP_002914.1:n.*71A>G
NM_002923.4:c.*71A>G MANE Select NP_002914.1:n.*71A>G
Search 100 bp 5'
Search 100 bp 3'