Linked Data
gnomAD v4:
5-37249548-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37249548T>C , CM000667.2:g.37249548T>C | GRCh38 |
| NC_000005.9:g.37249650T>C , CM000667.1:g.37249650T>C | GRCh37 |
| NC_000005.8:g.37285407T>C | NCBI36 |
| NG_032772.1:g.4881A>G | |
| NG_032772.2:g.4881A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925921.1:n.171+327T>C | ||
| NR_134263.1:n.176+327T>C |