Linked Data
gnomAD v4:
1-58576766-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58576766C>T , CM000663.2:g.58576766C>T | GRCh38 |
| NC_000001.10:g.59042438C>T , CM000663.1:g.59042438C>T | GRCh37 |
| NC_000001.9:g.58815026C>T | NCBI36 |
| NG_016237.1:g.5729G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371225.4:c.391G>A MANE Select | ENSP00000360269.2:p.Val131Met | |
| ENST00000371225.3:c.391G>A | ENSP00000360269.2:p.Val131Met | |
| NM_002353.2:c.391G>A | NP_002344.2:p.Val131Met | |
| NM_002353.3:c.391G>A MANE Select | NP_002344.2:p.Val131Met |