Canonical Allele Identifier: CA2649611421
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811742-G-GA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811744dup , CM000663.2:g.192811744dup GRCh38
NC_000001.10:g.192780874dup , CM000663.1:g.192780874dup GRCh37
NC_000001.9:g.191047497dup NCBI36
NG_012800.1:g.7706dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*148dup MANE Select ENSP00000235382.5:n.*148dup
ENST00000235382.6:c.*148dup ENSP00000235382.5:n.*148dup
NM_002923.3:c.*148dup NP_002914.1:n.*148dup
NM_002923.4:c.*148dup MANE Select NP_002914.1:n.*148dup
Search 100 bp 5'
Search 100 bp 3'