Canonical Allele Identifier: CA2649611473
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811816-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811816A>G , CM000663.2:g.192811816A>G GRCh38
NC_000001.10:g.192780946A>G , CM000663.1:g.192780946A>G GRCh37
NC_000001.9:g.191047569A>G NCBI36
NG_012800.1:g.7778A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*220A>G MANE Select ENSP00000235382.5:n.*220A>G
ENST00000235382.6:c.*220A>G ENSP00000235382.5:n.*220A>G
NM_002923.3:c.*220A>G NP_002914.1:n.*220A>G
NM_002923.4:c.*220A>G MANE Select NP_002914.1:n.*220A>G
Search 100 bp 5'
Search 100 bp 3'