Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46877496T>A , CM000685.2:g.46877496T>A | GRCh38 |
| NC_000023.10:g.46736931T>A , CM000685.1:g.46736931T>A | GRCh37 |
| NC_000023.9:g.46621875T>A | NCBI36 |
| NG_009107.1:g.45585T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006915.3:c.884-9T>A MANE Select | NP_008846.2:n.884-9T>A |
| ENST00000218340.4:c.884-9T>A MANE Select | ENSP00000218340.3:n.884-9T>A |
| NM_006915.2:c.884-9T>A | NP_008846.2:n.884-9T>A |
| ENST00000218340.3:c.884-9T>A | ENSP00000218340.3:n.884-9T>A |