Linked Data
gnomAD v4:
17-39688073-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39688073G>A , CM000679.2:g.39688073G>A | GRCh38 |
| NC_000017.10:g.37844326G>A , CM000679.1:g.37844326G>A | GRCh37 |
| NC_000017.9:g.35097852G>A | NCBI36 |
| NG_007503.1:g.4934G>A , LRG_724:g.4934G>A | |
| NG_034125.1:g.4998C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300658.8:c.-59C>T (PGAP3) | ENSP00000300658.4:n.-59C>T | |
| ENST00000584601.5:c.-638G>A (ERBB2) | ENSP00000462438.1:n.-638G>A | |
| ENST00000584856.1:c.-35-2054C>T (PGAP3) | ENSP00000463785.1:n.-35-2054C>T |