Canonical Allele Identifier: CA1146306349
Gene: RGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812063C= , CM000663.2:g.192812063C= GRCh38
NC_000001.10:g.192781193C= , CM000663.1:g.192781193C= GRCh37
NC_000001.9:g.191047816C= NCBI36
NG_012800.1:g.8025C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*467C= MANE Select ENSP00000235382.5:n.*467C=
ENST00000235382.6:c.*467C= ENSP00000235382.5:n.*467C=
NM_002923.3:c.*467C= NP_002914.1:n.*467C=
NM_002923.4:c.*467C= MANE Select NP_002914.1:n.*467C=
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