Canonical Allele Identifier: CA2649611628
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192812039-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812039C>G , CM000663.2:g.192812039C>G GRCh38
NC_000001.10:g.192781169C>G , CM000663.1:g.192781169C>G GRCh37
NC_000001.9:g.191047792C>G NCBI36
NG_012800.1:g.8001C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*443C>G MANE Select ENSP00000235382.5:n.*443C>G
ENST00000235382.6:c.*443C>G ENSP00000235382.5:n.*443C>G
NM_002923.3:c.*443C>G NP_002914.1:n.*443C>G
NM_002923.4:c.*443C>G MANE Select NP_002914.1:n.*443C>G
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