Canonical Allele Identifier: CA2574103248
Gene: RGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811655C>A , CM000663.2:g.192811655C>A GRCh38
NC_000001.10:g.192780785C>A , CM000663.1:g.192780785C>A GRCh37
NC_000001.9:g.191047408C>A NCBI36
NG_012800.1:g.7617C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*59C>A MANE Select ENSP00000235382.5:n.*59C>A
ENST00000235382.6:c.*59C>A ENSP00000235382.5:n.*59C>A
NM_002923.3:c.*59C>A NP_002914.1:n.*59C>A
NM_002923.4:c.*59C>A MANE Select NP_002914.1:n.*59C>A
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