Canonical Allele Identifier: CA528004639
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1256299222
gnomAD v2: 1-192780765-CT-C
MyVariant Identifiers: chr1:g.192780766del (hg19) chr1:g.192811636del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811640del , CM000663.2:g.192811640del GRCh38
NC_000001.10:g.192780770del , CM000663.1:g.192780770del GRCh37
NC_000001.9:g.191047393del NCBI36
NG_012800.1:g.7602del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*44del MANE Select ENSP00000235382.5:n.*44del
ENST00000235382.6:c.*44del ENSP00000235382.5:n.*44del
NM_002923.3:c.*44del NP_002914.1:n.*44del
NM_002923.4:c.*44del MANE Select NP_002914.1:n.*44del
Search 100 bp 5'
Search 100 bp 3'