Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.71572326T>C , CM000678.2:g.71572326T>C | GRCh38 |
| NC_000016.9:g.71606229T>C , CM000678.1:g.71606229T>C | GRCh37 |
| NC_000016.8:g.70163730T>C | NCBI36 |
| NG_008235.1:g.9770A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000353.3:c.568-2A>G (TAT) MANE Select | NP_000344.1:n.568-2A>G |
| ENST00000355962.5:c.568-2A>G (TAT) MANE Select | ENSP00000348234.4:n.568-2A>G |
| NM_000353.2:c.568-2A>G (TAT) | NP_000344.1:n.568-2A>G |
| NR_103851.1:n.591T>C (TAT-AS1) | |
| NR_103852.1:n.565T>C (TAT-AS1) | |
| ENST00000355962.4:c.568-2A>G (TAT) | ENSP00000348234.4:n.568-2A>G |