Linked Data
gnomAD v4:
X-153690468-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153690468G>T , CM000685.2:g.153690468G>T | GRCh38 |
| NC_000023.10:g.152955923G>T , CM000685.1:g.152955923G>T | GRCh37 |
| NC_000023.9:g.152609117G>T | NCBI36 |
| NG_012016.1:g.7172G>T | |
| NG_012016.2:g.7172G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.356G>T MANE Select | ENSP00000253122.5:p.Gly119Val | |
| ENST00000675713.1:n.110G>T | ||
| ENST00000253122.9:c.356G>T | ENSP00000253122.5:p.Gly119Val | |
| ENST00000430077.6:c.11G>T | ENSP00000403041.2:p.Gly4Val | |
| ENST00000476466.1:n.208G>T | ||
| NM_001142805.1:c.356G>T | NP_001136277.1:p.Gly119Val | |
| NM_001142806.1:c.11G>T | NP_001136278.1:p.Gly4Val | |
| NM_005629.3:c.356G>T | NP_005620.1:p.Gly119Val | |
| NM_005629.4:c.356G>T MANE Select | NP_005620.1:p.Gly119Val | |
| NM_001142805.2:c.356G>T | NP_001136277.1:p.Gly119Val |