Canonical Allele Identifier: CA2747137513
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811692dup , CM000663.2:g.192811692dup GRCh38
NC_000001.10:g.192780822dup , CM000663.1:g.192780822dup GRCh37
NC_000001.9:g.191047445dup NCBI36
NG_012800.1:g.7654dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*96dup MANE Select ENSP00000235382.5:n.*96dup
ENST00000235382.6:c.*96dup ENSP00000235382.5:n.*96dup
NM_002923.3:c.*96dup NP_002914.1:n.*96dup
NM_002923.4:c.*96dup MANE Select NP_002914.1:n.*96dup