Linked Data
MyVariant Identifiers:
chr16:g.222926T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172927T>G , CM000678.2:g.172927T>G | GRCh38 |
| NC_000016.9:g.222926T>G , CM000678.1:g.222926T>G | GRCh37 |
| NC_000016.8:g.162926T>G | NCBI36 |
| NG_000006.1:g.33790T>G | |
| NG_059186.1:g.1277T>G | |
| NG_059271.1:g.5081T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.15T>G MANE Select | ENSP00000251595.6:p.Pro5= | |
| ENST00000251595.10:c.15T>G | ENSP00000251595.6:p.Pro5= | |
| ENST00000397806.1:c.-33T>G | ENSP00000380908.1:n.-33T>G | |
| ENST00000482565.1:n.34T>G | ||
| NM_000517.4:c.15T>G | NP_000508.1:p.Pro5= | |
| NM_000517.6:c.15T>G MANE Select | NP_000508.1:p.Pro5= |