Canonical Allele Identifier: CA2571826689
Gene: RGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811852dup , CM000663.2:g.192811852dup GRCh38
NC_000001.10:g.192780982dup , CM000663.1:g.192780982dup GRCh37
NC_000001.9:g.191047605dup NCBI36
NG_012800.1:g.7814dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*256dup MANE Select ENSP00000235382.5:n.*256dup
ENST00000235382.6:c.*256dup ENSP00000235382.5:n.*256dup
NM_002923.3:c.*256dup NP_002914.1:n.*256dup
NM_002923.4:c.*256dup MANE Select NP_002914.1:n.*256dup
Search 100 bp 5'
Search 100 bp 3'