Canonical Allele Identifier: CA2561223162
Gene: RGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811863A>G , CM000663.2:g.192811863A>G GRCh38
NC_000001.10:g.192780993A>G , CM000663.1:g.192780993A>G GRCh37
NC_000001.9:g.191047616A>G NCBI36
NG_012800.1:g.7825A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*267A>G MANE Select ENSP00000235382.5:n.*267A>G
ENST00000235382.6:c.*267A>G ENSP00000235382.5:n.*267A>G
NM_002923.3:c.*267A>G NP_002914.1:n.*267A>G
NM_002923.4:c.*267A>G MANE Select NP_002914.1:n.*267A>G
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Search 100 bp 3'