Linked Data
gnomAD v4:
21-43169021-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43169021C>A , CM000683.2:g.43169021C>A | GRCh38 |
| NG_009823.1:g.4991C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291554.6:c.-79C>A MANE Select | ENSP00000291554.2:n.-79C>A | |
| NM_000394.3:c.-79C>A | NP_000385.1:n.-79C>A | |
| XR_001755073.1:n.647+2016G>T | ||
| NM_000394.4:c.-79C>A MANE Select | NP_000385.1:n.-79C>A |