Canonical Allele Identifier: CA2649611391
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811697-GTTC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811698_192811700del , CM000663.2:g.192811698_192811700del GRCh38
NC_000001.10:g.192780828_192780830del , CM000663.1:g.192780828_192780830del GRCh37
NC_000001.9:g.191047451_191047453del NCBI36
NG_012800.1:g.7660_7662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*102_*104del MANE Select ENSP00000235382.5:n.*102_*104del
ENST00000235382.6:c.*102_*104del ENSP00000235382.5:n.*102_*104del
NM_002923.3:c.*102_*104del NP_002914.1:n.*102_*104del
NM_002923.4:c.*102_*104del MANE Select NP_002914.1:n.*102_*104del
Search 100 bp 5'
Search 100 bp 3'