Linked Data
gnomAD v4:
1-58576751-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58576751T>C , CM000663.2:g.58576751T>C | GRCh38 |
| NC_000001.10:g.59042423T>C , CM000663.1:g.59042423T>C | GRCh37 |
| NC_000001.9:g.58815011T>C | NCBI36 |
| NG_016237.1:g.5744A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371225.4:c.406A>G MANE Select | ENSP00000360269.2:p.Thr136Ala | |
| ENST00000371225.3:c.406A>G | ENSP00000360269.2:p.Thr136Ala | |
| NM_002353.2:c.406A>G | NP_002344.2:p.Thr136Ala | |
| NM_002353.3:c.406A>G MANE Select | NP_002344.2:p.Thr136Ala |