Linked Data
gnomAD v4:
17-42404706-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42404706T>A , CM000679.2:g.42404706T>A | GRCh38 |
| NC_000017.10:g.40556724T>A , CM000679.1:g.40556724T>A | GRCh37 |
| NC_000017.9:g.37810250T>A | NCBI36 |
| NG_015845.1:g.23615A>T | |
| NG_015845.2:g.23615A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357037.6:c.1154A>T MANE Select | ENSP00000349541.4:p.Asp385Val | |
| ENST00000357037.5:c.1154A>T | ENSP00000349541.4:p.Asp385Val | |
| NM_012232.5:c.1154A>T | NP_036364.2:p.Asp385Val | |
| NM_012232.6:c.1154A>T MANE Select | NP_036364.2:p.Asp385Val |