Canonical Allele Identifier: CA2649611409
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811726-TTCAAA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811727_192811731del , CM000663.2:g.192811727_192811731del GRCh38
NC_000001.10:g.192780857_192780861del , CM000663.1:g.192780857_192780861del GRCh37
NC_000001.9:g.191047480_191047484del NCBI36
NG_012800.1:g.7689_7693del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*131_*135del MANE Select ENSP00000235382.5:n.*131_*135del
ENST00000235382.6:c.*131_*135del ENSP00000235382.5:n.*131_*135del
NM_002923.3:c.*131_*135del NP_002914.1:n.*131_*135del
NM_002923.4:c.*131_*135del MANE Select NP_002914.1:n.*131_*135del
Search 100 bp 5'
Search 100 bp 3'