Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.71570766A>T , CM000678.2:g.71570766A>T | GRCh38 |
| NC_000016.9:g.71604669A>T , CM000678.1:g.71604669A>T | GRCh37 |
| NC_000016.8:g.70162170A>T | NCBI36 |
| NG_008235.1:g.11330T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000353.3:c.825T>A (TAT) MANE Select | NP_000344.1:p.Cys275Ter |
| ENST00000355962.5:c.825T>A (TAT) MANE Select | ENSP00000348234.4:p.Cys275Ter |
| NM_000353.2:c.825T>A (TAT) | NP_000344.1:p.Cys275Ter |
| NR_103851.1:n.285-1254A>T (TAT-AS1) | |
| NR_103852.1:n.259-1254A>T (TAT-AS1) | |
| ENST00000355962.4:c.825T>A (TAT) | ENSP00000348234.4:p.Cys275Ter |