Linked Data
dbSNP Id:
rs2118504524
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.103262083T>C , CM000671.2:g.103262083T>C | GRCh38 |
| NC_000009.11:g.106024365T>C , CM000671.1:g.106024365T>C | GRCh37 |
| NC_000009.10:g.105064186T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_121578.1:n.771+2441A>G |