Canonical Allele Identifier: CA2747137541
Gene: RGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812174C>G , CM000663.2:g.192812174C>G GRCh38
NC_000001.10:g.192781304C>G , CM000663.1:g.192781304C>G GRCh37
NC_000001.9:g.191047927C>G NCBI36
NG_012800.1:g.8136C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*578C>G MANE Select ENSP00000235382.5:n.*578C>G
ENST00000235382.6:c.*578C>G ENSP00000235382.5:n.*578C>G
NM_002923.3:c.*578C>G NP_002914.1:n.*578C>G
NM_002923.4:c.*578C>G MANE Select NP_002914.1:n.*578C>G
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