Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436296G>A , CM000678.2:g.67436296G>A | GRCh38 |
| NC_000016.9:g.67470199G>A , CM000678.1:g.67470199G>A | GRCh37 |
| NC_000016.8:g.66027700G>A | NCBI36 |
| NG_011482.1:g.49891C>T | |
| NG_016549.1:g.10164G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.712G>A MANE Select | ENSP00000316786.5:p.Ala238Thr | |
| ENST00000326152.5:c.712G>A | ENSP00000316786.5:p.Ala238Thr | |
| NM_000196.3:c.712G>A | NP_000187.3:p.Ala238Thr | |
| NM_000196.4:c.712G>A MANE Select | NP_000187.3:p.Ala238Thr |