Linked Data
gnomAD v4:
5-37249527-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37249527C>T , CM000667.2:g.37249527C>T | GRCh38 |
| NC_000005.9:g.37249629C>T , CM000667.1:g.37249629C>T | GRCh37 |
| NC_000005.8:g.37285386C>T | NCBI36 |
| NG_032772.1:g.4902G>A | |
| NG_032772.2:g.4902G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925921.1:n.171+306C>T | ||
| NR_134263.1:n.176+306C>T |