Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2621145T>A , CM000671.2:g.2621145T>A | GRCh38 |
| NC_000009.11:g.2621145T>A , CM000671.1:g.2621145T>A | GRCh37 |
| NC_000009.10:g.2611145T>A | NCBI36 |
| NG_012741.1:g.4353T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_015375.2:n.274+955A>T |