Canonical Allele Identifier: CA35070406
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs746604577
gnomAD v2: 1-192781354-G-C
gnomAD v3: 1-192812224-G-C
gnomAD v4: 1-192812224-G-C
MyVariant Identifiers: chr1:g.192781354G>C (hg19) chr1:g.192812224G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812224G>C , CM000663.2:g.192812224G>C GRCh38
NC_000001.10:g.192781354G>C , CM000663.1:g.192781354G>C GRCh37
NC_000001.9:g.191047977G>C NCBI36
NG_012800.1:g.8186G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*628G>C MANE Select ENSP00000235382.5:n.*628G>C
ENST00000235382.6:c.*628G>C ENSP00000235382.5:n.*628G>C
NM_002923.3:c.*628G>C NP_002914.1:n.*628G>C
NM_002923.4:c.*628G>C MANE Select NP_002914.1:n.*628G>C
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