Linked Data
gnomAD v4:
21-31659387-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31659387C>A , CM000683.2:g.31659387C>A | GRCh38 |
| NC_000021.8:g.33031700C>A , CM000683.1:g.33031700C>A | GRCh37 |
| NC_000021.7:g.31953571C>A | NCBI36 |
| NG_008689.1:g.4766C>A , LRG_652:g.4766C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_430363.2:n.124+10G>T | ||
| XR_937662.1:n.124+10G>T | ||
| XR_002958653.1:n.88+10G>T | ||
| XR_430363.3:n.159+10G>T |