Linked Data
gnomAD v4:
X-108084777-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108084777A>T , CM000685.2:g.108084777A>T | GRCh38 |
| NC_000023.10:g.107328007A>T , CM000685.1:g.107328007A>T | GRCh37 |
| NC_000023.9:g.107214663A>T | NCBI36 |
| NG_012521.1:g.11842T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217958.8:c.*197T>A MANE Select | ENSP00000217958.3:n.*197T>A | |
| ENST00000217958.7:c.*197T>A | ENSP00000217958.3:n.*197T>A | |
| ENST00000372295.5:c.*197T>A | ENSP00000361369.1:n.*197T>A | |
| ENST00000372296.5:c.*343T>A | ENSP00000361370.1:n.*343T>A | |
| NM_002814.3:c.*197T>A | NP_002805.1:n.*197T>A | |
| NM_170750.2:c.*343T>A | NP_736606.1:n.*343T>A | |
| NM_002814.4:c.*197T>A MANE Select | NP_002805.1:n.*197T>A | |
| NM_170750.3:c.*343T>A | NP_736606.1:n.*343T>A |