Canonical Allele Identifier: CA2649611465
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811805-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811805C>T , CM000663.2:g.192811805C>T GRCh38
NC_000001.10:g.192780935C>T , CM000663.1:g.192780935C>T GRCh37
NC_000001.9:g.191047558C>T NCBI36
NG_012800.1:g.7767C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*209C>T MANE Select ENSP00000235382.5:n.*209C>T
ENST00000235382.6:c.*209C>T ENSP00000235382.5:n.*209C>T
NM_002923.3:c.*209C>T NP_002914.1:n.*209C>T
NM_002923.4:c.*209C>T MANE Select NP_002914.1:n.*209C>T
Search 100 bp 5'
Search 100 bp 3'