Canonical Allele Identifier: CA35070375
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs12566194
gnomAD v2: 1-192781090-A-T
gnomAD v3: 1-192811960-A-T
gnomAD v4: 1-192811960-A-T
MyVariant Identifiers: chr1:g.192781090A>T (hg19) chr1:g.192811960A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811960A>T , CM000663.2:g.192811960A>T GRCh38
NC_000001.10:g.192781090A>T , CM000663.1:g.192781090A>T GRCh37
NC_000001.9:g.191047713A>T NCBI36
NG_012800.1:g.7922A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*364A>T MANE Select ENSP00000235382.5:n.*364A>T
ENST00000235382.6:c.*364A>T ENSP00000235382.5:n.*364A>T
NM_002923.3:c.*364A>T NP_002914.1:n.*364A>T
NM_002923.4:c.*364A>T MANE Select NP_002914.1:n.*364A>T
Search 100 bp 5'
Search 100 bp 3'