Linked Data
dbSNP Id:
rs1951113099
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46897396A>T , CM000675.2:g.46897396A>T | GRCh38 |
| NC_000013.10:g.47471531A>T , CM000675.1:g.47471531A>T | GRCh37 |
| NC_000013.9:g.46369532A>T | NCBI36 |
| NG_013011.1:g.4639T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001378924.1:c.-329+556T>A | NP_001365853.1:n.-329+556T>A |