Canonical Allele Identifier: CA729320673
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1335514547
MyVariant Identifiers: chr1:g.192781306G>A (hg19) chr1:g.192812176G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812176G>A , CM000663.2:g.192812176G>A GRCh38
NC_000001.10:g.192781306G>A , CM000663.1:g.192781306G>A GRCh37
NC_000001.9:g.191047929G>A NCBI36
NG_012800.1:g.8138G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*580G>A MANE Select ENSP00000235382.5:n.*580G>A
ENST00000235382.6:c.*580G>A ENSP00000235382.5:n.*580G>A
NM_002923.3:c.*580G>A NP_002914.1:n.*580G>A
NM_002923.4:c.*580G>A MANE Select NP_002914.1:n.*580G>A
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