Linked Data
MyVariant Identifiers:
chr16:g.222977T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172978T>G , CM000678.2:g.172978T>G | GRCh38 |
| NC_000016.9:g.222977T>G , CM000678.1:g.222977T>G | GRCh37 |
| NC_000016.8:g.162977T>G | NCBI36 |
| NG_000006.1:g.33841T>G | |
| NG_059186.1:g.1328T>G | |
| NG_059271.1:g.5132T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.66T>G MANE Select | ENSP00000251595.6:p.Ala22= | |
| ENST00000251595.10:c.66T>G | ENSP00000251595.6:p.Ala22= | |
| ENST00000397806.1:c.-2+20T>G | ENSP00000380908.1:n.-2+20T>G | |
| ENST00000482565.1:n.85T>G | ||
| ENST00000484216.1:n.35T>G | ||
| NM_000517.4:c.66T>G | NP_000508.1:p.Ala22= | |
| NM_000517.6:c.66T>G MANE Select | NP_000508.1:p.Ala22= |