Linked Data
dbSNP Id:
rs1951112442
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46897295del , CM000675.2:g.46897295del | GRCh38 |
| NC_000013.10:g.47471430del , CM000675.1:g.47471430del | GRCh37 |
| NC_000013.9:g.46369431del | NCBI36 |
| NG_013011.1:g.4740del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_001378924.1:c.-329+657del | NP_001365853.1:n.-329+657del |