Canonical Allele Identifier: CA729320439
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1373813754
MyVariant Identifiers: chr1:g.192780772C>T (hg19) chr1:g.192811642C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811642C>T , CM000663.2:g.192811642C>T GRCh38
NC_000001.10:g.192780772C>T , CM000663.1:g.192780772C>T GRCh37
NC_000001.9:g.191047395C>T NCBI36
NG_012800.1:g.7604C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*46C>T MANE Select ENSP00000235382.5:n.*46C>T
ENST00000235382.6:c.*46C>T ENSP00000235382.5:n.*46C>T
NM_002923.3:c.*46C>T NP_002914.1:n.*46C>T
NM_002923.4:c.*46C>T MANE Select NP_002914.1:n.*46C>T
Search 100 bp 5'
Search 100 bp 3'