Canonical Allele Identifier: CA2649611381
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811672-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811672G>C , CM000663.2:g.192811672G>C GRCh38
NC_000001.10:g.192780802G>C , CM000663.1:g.192780802G>C GRCh37
NC_000001.9:g.191047425G>C NCBI36
NG_012800.1:g.7634G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*76G>C MANE Select ENSP00000235382.5:n.*76G>C
ENST00000235382.6:c.*76G>C ENSP00000235382.5:n.*76G>C
NM_002923.3:c.*76G>C NP_002914.1:n.*76G>C
NM_002923.4:c.*76G>C MANE Select NP_002914.1:n.*76G>C
Search 100 bp 5'
Search 100 bp 3'