Linked Data
gnomAD v4:
1-17393959-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17393959T>G , CM000663.2:g.17393959T>G | GRCh38 |
| NC_000001.10:g.17720455T>G , CM000663.1:g.17720455T>G | GRCh37 |
| NC_000001.9:g.17593042T>G | NCBI36 |
| NG_032943.1:g.26714T>G | |
| NG_032943.2:g.26714T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000619609.1:c.1075-16T>G MANE Select | ENSP00000483125.1:n.1075-16T>G | |
| NM_207421.4:c.1075-16T>G MANE Select | NP_997304.3:n.1075-16T>G |