Canonical Allele Identifier: CA2649611439
Gene: RGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-192811764-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811764C>A , CM000663.2:g.192811764C>A GRCh38
NC_000001.10:g.192780894C>A , CM000663.1:g.192780894C>A GRCh37
NC_000001.9:g.191047517C>A NCBI36
NG_012800.1:g.7726C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*168C>A MANE Select ENSP00000235382.5:n.*168C>A
ENST00000235382.6:c.*168C>A ENSP00000235382.5:n.*168C>A
NM_002923.3:c.*168C>A NP_002914.1:n.*168C>A
NM_002923.4:c.*168C>A MANE Select NP_002914.1:n.*168C>A
Search 100 bp 5'
Search 100 bp 3'