Linked Data
gnomAD v4:
12-65964388-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65964388T>A , CM000674.2:g.65964388T>A | GRCh38 |
| NC_000012.11:g.66358168T>A , CM000674.1:g.66358168T>A | GRCh37 |
| NC_000012.10:g.64644435T>A | NCBI36 |
| NG_016296.1:g.144929T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403681.7:c.*1096T>A MANE Select | ENSP00000384026.2:n.*1096T>A | |
| ENST00000403681.6:c.*1096T>A | ENSP00000384026.2:n.*1096T>A | |
| NM_003483.4:c.*1096T>A | NP_003474.1:n.*1096T>A | |
| NM_003483.6:c.*1096T>A MANE Select | NP_003474.1:n.*1096T>A |