Linked Data
gnomAD v4:
13-46897175-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46897175T>C , CM000675.2:g.46897175T>C | GRCh38 |
| NC_000013.10:g.47471310T>C , CM000675.1:g.47471310T>C | GRCh37 |
| NC_000013.9:g.46369311T>C | NCBI36 |
| NG_013011.1:g.4860A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001378924.1:c.-329+777A>G | NP_001365853.1:n.-329+777A>G |