Canonical Allele Identifier: CA528004641
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs12084818
gnomAD v2: 1-192780913-G-T
gnomAD v3: 1-192811783-G-T
gnomAD v4: 1-192811783-G-T
MyVariant Identifiers: chr1:g.192780913G>T (hg19) chr1:g.192811783G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811783G>T , CM000663.2:g.192811783G>T GRCh38
NC_000001.10:g.192780913G>T , CM000663.1:g.192780913G>T GRCh37
NC_000001.9:g.191047536G>T NCBI36
NG_012800.1:g.7745G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*187G>T MANE Select ENSP00000235382.5:n.*187G>T
ENST00000235382.6:c.*187G>T ENSP00000235382.5:n.*187G>T
NM_002923.3:c.*187G>T NP_002914.1:n.*187G>T
NM_002923.4:c.*187G>T MANE Select NP_002914.1:n.*187G>T
Search 100 bp 5'
Search 100 bp 3'