Linked Data
gnomAD v4:
4-177442568-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442568T>G , CM000666.2:g.177442568T>G | GRCh38 |
| NC_000004.11:g.178363722T>G , CM000666.1:g.178363722T>G | GRCh37 |
| NC_000004.10:g.178600716T>G | NCBI36 |
| NG_011845.2:g.4936A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741929.1:n.69T>G |