Linked Data
gnomAD v4:
2-72891694-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.72891697del , CM000664.2:g.72891697del | GRCh38 |
| NC_000002.11:g.73118826del , CM000664.1:g.73118826del | GRCh37 |
| NC_000002.10:g.72972334del | NCBI36 |
| NG_008234.1:g.9315del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234454.6:c.*160del MANE Select | ENSP00000234454.5:n.*160del | |
| ENST00000234454.5:c.*160del | ENSP00000234454.5:n.*160del | |
| ENST00000498749.1:n.891del | ||
| NM_003124.4:c.*160del | NP_003115.1:n.*160del | |
| NM_003124.5:c.*160del MANE Select | NP_003115.1:n.*160del |