Linked Data
gnomAD v4:
13-46897122-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46897122A>G , CM000675.2:g.46897122A>G | GRCh38 |
| NC_000013.10:g.47471257A>G , CM000675.1:g.47471257A>G | GRCh37 |
| NC_000013.9:g.46369258A>G | NCBI36 |
| NG_013011.1:g.4913T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001378924.1:c.-329+830T>C | NP_001365853.1:n.-329+830T>C |