Linked Data
gnomAD v4:
16-172970-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172970G>T , CM000678.2:g.172970G>T | GRCh38 |
| NC_000016.9:g.222969G>T , CM000678.1:g.222969G>T | GRCh37 |
| NC_000016.8:g.162969G>T | NCBI36 |
| NG_000006.1:g.33833G>T | |
| NG_059186.1:g.1320G>T | |
| NG_059271.1:g.5124G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.58G>T MANE Select | ENSP00000251595.6:p.Ala20Ser | |
| ENST00000251595.10:c.58G>T | ENSP00000251595.6:p.Ala20Ser | |
| ENST00000397806.1:c.-2+12G>T | ENSP00000380908.1:n.-2+12G>T | |
| ENST00000482565.1:n.77G>T | ||
| ENST00000484216.1:n.27G>T | ||
| NM_000517.4:c.58G>T | NP_000508.1:p.Ala20Ser | |
| NM_000517.6:c.58G>T MANE Select | NP_000508.1:p.Ala20Ser |