Linked Data
MyVariant Identifiers:
chr16:g.223488G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173489G>T , CM000678.2:g.173489G>T | GRCh38 |
| NC_000016.9:g.223488G>T , CM000678.1:g.223488G>T | GRCh37 |
| NC_000016.8:g.163488G>T | NCBI36 |
| NG_000006.1:g.34352G>T | |
| NG_059186.1:g.1839G>T | |
| NG_059271.1:g.5643G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000251595.11:c.318G>T MANE Select | ENSP00000251595.6:p.Leu106= | |
| ENST00000251595.10:c.318G>T | ENSP00000251595.6:p.Leu106= | |
| ENST00000397806.1:c.222G>T | ENSP00000380908.1:p.Leu74= | |
| ENST00000482565.1:n.454G>T | ||
| NM_000517.4:c.318G>T | NP_000508.1:p.Leu106= | |
| NM_000517.6:c.318G>T MANE Select | NP_000508.1:p.Leu106= |