Linked Data
dbSNP Id:
rs12035879
gnomAD v2:
1-163142555-G-A
gnomAD v3:
1-163172765-G-A
gnomAD v4:
1-163172765-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.163172765G>A , CM000663.2:g.163172765G>A | GRCh38 |
| NC_000001.10:g.163142555G>A , CM000663.1:g.163142555G>A | GRCh37 |
| NC_000001.9:g.161409179G>A | NCBI36 |
| NG_027731.1:g.35409C>T | |
| NG_027731.2:g.154027C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000313961.10:c.45-4397C>T (RGS5) MANE Select | ENSP00000319308.5:n.45-4397C>T | |
| ENST00000313961.9:c.45-4397C>T (RGS5) | ENSP00000319308.5:n.45-4397C>T | |
| ENST00000367903.7:c.70-173C>T (RGS5) | ENSP00000356879.3:n.70-173C>T | |
| ENST00000428971.2:n.447-4397C>T (RGS5) | ||
| ENST00000525894.5:n.125-4397C>T (RGS5) | ||
| ENST00000527988.1:c.-107-20049C>T (RGS5) | ENSP00000432313.1:n.-107-20049C>T | |
| ENST00000530241.5:n.297-4397C>T (RGS5) | ||
| ENST00000530507.5:c.45-4397C>T (RGS5) | ENSP00000433001.1:n.45-4397C>T | |
| ENST00000531476.1:c.45-10789C>T (RGS5) | ENSP00000435861.1:n.45-10789C>T | |
| ENST00000531954.5:n.212-4397C>T (RGS5) | ||
| ENST00000534288.5:n.352-4397C>T (RGS5) | ||
| ENST00000618415.4:c.-280-4397C>T (RGS5) | ENSP00000480891.1:n.-280-4397C>T | |
| NM_001195303.2:c.-107-20049C>T (RGS5) | NP_001182232.1:n.-107-20049C>T | |
| NM_001254748.1:c.-280-4397C>T (RGS5) | NP_001241677.1:n.-280-4397C>T | |
| NM_001254749.1:c.45-4397C>T (RGS5) | NP_001241678.1:n.45-4397C>T | |
| NM_003617.3:c.45-4397C>T (RGS5) | NP_003608.1:n.45-4397C>T | |
| NR_110699.1:n.258+9889G>A (RGS5-AS1) | ||
| NM_003617.4:c.45-4397C>T (RGS5) MANE Select | NP_003608.1:n.45-4397C>T | |
| NM_001195303.3:c.-107-20049C>T (RGS5) | NP_001182232.1:n.-107-20049C>T | |
| NM_001254749.2:c.45-4397C>T (RGS5) | NP_001241678.1:n.45-4397C>T | |
| NM_001254748.2:c.-280-4397C>T (RGS5) | NP_001241677.1:n.-280-4397C>T |