Linked Data
gnomAD v4:
13-46897158-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46897158T>C , CM000675.2:g.46897158T>C | GRCh38 |
| NC_000013.10:g.47471293T>C , CM000675.1:g.47471293T>C | GRCh37 |
| NC_000013.9:g.46369294T>C | NCBI36 |
| NG_013011.1:g.4877A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001378924.1:c.-329+794A>G | NP_001365853.1:n.-329+794A>G |