Linked Data
gnomAD v4:
1-94021321-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94021321T>A , CM000663.2:g.94021321T>A | GRCh38 |
| NC_000001.10:g.94486877T>A , CM000663.1:g.94486877T>A | GRCh37 |
| NC_000001.9:g.94259465T>A | NCBI36 |
| NG_009073.1:g.104829A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4937A>T MANE Select | ENSP00000359245.3:p.Asp1646Val | |
| ENST00000370225.3:c.4937A>T | ENSP00000359245.3:p.Asp1646Val | |
| ENST00000460514.1:n.431A>T | ||
| ENST00000470771.1:n.47A>T | ||
| ENST00000536513.5:c.1313A>T | ENSP00000439707.2:p.Asp438Val | |
| NM_000350.2:c.4937A>T | NP_000341.2:p.Asp1646Val | |
| NM_000350.3:c.4937A>T MANE Select | NP_000341.2:p.Asp1646Val |