Linked Data
gnomAD v4:
1-93997950-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.93997950A>T , CM000663.2:g.93997950A>T | GRCh38 |
| NC_000001.10:g.94463506A>T , CM000663.1:g.94463506A>T | GRCh37 |
| NC_000001.9:g.94236094A>T | NCBI36 |
| NG_009073.1:g.128200T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6640T>A MANE Select | ENSP00000359245.3:p.Ser2214Thr | |
| ENST00000370225.3:c.6640T>A | ENSP00000359245.3:p.Ser2214Thr | |
| ENST00000536513.5:c.3016T>A | ENSP00000439707.2:p.Ser1006Thr | |
| NM_000350.2:c.6640T>A | NP_000341.2:p.Ser2214Thr | |
| NM_000350.3:c.6640T>A MANE Select | NP_000341.2:p.Ser2214Thr |