Canonical Allele Identifier: CA35070350
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs558660303
gnomAD v3: 1-192811660-A-C
gnomAD v4: 1-192811660-A-C
MyVariant Identifiers: chr1:g.192780790A>C (hg19) chr1:g.192811660A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811660A>C , CM000663.2:g.192811660A>C GRCh38
NC_000001.10:g.192780790A>C , CM000663.1:g.192780790A>C GRCh37
NC_000001.9:g.191047413A>C NCBI36
NG_012800.1:g.7622A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*64A>C MANE Select ENSP00000235382.5:n.*64A>C
ENST00000235382.6:c.*64A>C ENSP00000235382.5:n.*64A>C
NM_002923.3:c.*64A>C NP_002914.1:n.*64A>C
NM_002923.4:c.*64A>C MANE Select NP_002914.1:n.*64A>C
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